Lupin Pharmaceuticals, Inc. LUPIN LIMITED LUPIN LIMITED

cephalexin Cephalexin CEPHALEXIN CEPHALEXIN ANHYDROUS FD&C RED NO. 40 SILICON DIOXIDE SODIUM BENZOATE STRAWBERRY SUCROSE XANTHAN GUM Pink Strawberry cephalexin Cephalexin CEPHALEXIN CEPHALEXIN ANHYDROUS FD&C RED NO. 40 SILICON DIOXIDE SODIUM BENZOATE STRAWBERRY SUCROSE XANTHAN GUM Pink Strawberry cephalexin Cephalexin CEPHALEXIN CEPHALEXIN ANHYDROUS FD&C RED NO. 40 SILICON DIOXIDE SODIUM BENZOATE STRAWBERRY SUCROSE XANTHAN GUM Pink Strawberry cephalexin Cephalexin CEPHALEXIN CEPHALEXIN ANHYDROUS FD&C RED NO. 40 SILICON DIOXIDE SODIUM BENZOATE STRAWBERRY SUCROSE XANTHAN GUM Pink Strawberry

Indications and Usage (1)                 3/2026 Dosage and Administration (2)         3/2026

Cephalexin USP is a cephalosporin antibacterial drug indicated for the treatment of the following infections caused by susceptible isolates of designated bacteria in adults and pediatric patients aged one year and older: Respiratory tract infection (1.1) Otitis media (1.2) Skin and skin structure infections (1.3) Bone infections (1.4) Genitourinary tract infections (1.5) To reduce the development of drug-resistant bacteria and maintain the effectiveness of cephalexin and other antibacterial drugs, cephalexin for oral suspension should be used only to treat infections that are proven or strongly suspected to be caused by bacteria. (1.6)

Cephalexin for oral suspension is indicated for the treatment of respiratory tract infections caused by susceptible isolates of Streptococcus pneumoniae and Streptococcus pyogenes in adults and pediatric patients aged one year and older.

Cephalexin for oral suspension is indicated for the treatment of otitis media caused by susceptible isolates of Streptococcus pneumoniae, Haemophilus influenzae, Staphylococcus aureus, Streptococcus pyogenes, and Moraxella catarrhalis in adults and pediatric patients aged one year and older.

Cephalexin for oral suspension is indicated for the treatment of skin and skin structure infections caused by susceptible isolates of the following Gram-positive bacteria: Staphylococcus aureus and Streptococcus pyogenes in adults and pediatric patients aged one year and older.

Cephalexin for oral suspension is indicated for the treatment of bone infections caused by susceptible isolates of Staphylococcus aureus and Proteus mirabilis in adults and pediatric patients aged one year and older.

Cephalexin for oral suspension is indicated for the treatment of genitourinary tract infections, including acute prostatitis, caused by susceptible isolates of Escherichia coli, Proteus mirabilis, and Klebsiella pneumoniae in adults and pediatric patients aged one year and older.

To reduce the development of drug-resistant bacteria and maintain the effectiveness of cephalexin for oral suspension and other antibacterial drugs, cephalexin for oral suspension should be used only to treat infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information is available, this information should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy.

Adults and patients at least 15 years of age	The usual dose is 250 mg every 6 hours, but a dose of 500 mg every 12 hours may be administered (2.1).
Pediatric patients (over 1 year of age)	•    Otitis media: 75 to 100 mg/kg in equally divided doses every 6 hours (2.2) •    All other indications: 25 to 50 mg/kg given in equally divided doses (2.2) •    In severe infections: 50 to 100 mg/kg may be administered in equally divided doses (2.2)

Duration of therapy ranges from 7 to 14 days depending on the infection type and severity. (2) See full prescribing information directions for mixing cephalexin for oral suspension (2.3) Dosage adjustment is required in patients with severe and end stage renal disease (ESRD) defined as creatinine clearance below 30 mL/min. (2.4)

The recommended dosage of oral cephalexin is 250 mg every 6 hours, but a dose of 500 mg every 12 hours may be administered. Treatment is administered for 7 to 14 days. For more severe infections larger doses of oral cephalexin may be needed, up to 4 grams daily in two to four equally divided doses.

The recommended total daily dose of oral cephalexin for pediatric patients is 25 to 50 mg/kg given in equally divided doses for 7 to 14 days. In the treatment of β-hemolytic streptococcal infections, duration of at least 10 days is recommended. In severe infections, a total daily dose of 50 to 100 mg/kg may be administered in equally divided doses. For the treatment of otitis media, the recommended daily dose is 75 to 100 mg/kg given in equally divided doses. See Table 1 for the dosage of Cephalexin for oral suspension by weight for pediatric patients.

Table 1: Dosage by Weight of Cephalexin for Oral Suspension for Pediatric Patients  

*teaspoon =tsp
Weight of Pediatric Patient	Cephalexin for Oral Suspension (125 mg/5mL)	Cephalexin for Oral Suspension (250 mg/5mL)
OPTION 1	Dosage	Dosage
10 kg	½ to 1 tsp* four times a day	¼ to ½ tsp four times a day
20 kg	1 to 2 tsp four times a day	½ to 1 tsp four times a day
40 kg	2 to 4 tsp four times a day	1 to 2 tsp four times a day
OPTION 2
10 kg	1 to 2 tsp two times a day	½ to 1 tsp two times a day
20 kg	2 to 4 tsp two times a day	1 to 2 tsp two times a day
40 kg	2 to 4 tsp two times a day	2 to 4 tsp two times a day

125 mg/5 mL (100 mL when mixed): Prepare suspension time at dispensing. Add to the bottle a total of 69 mL of water. For ease in preparation, tap bottle to loosen powder, add the water in 2 portions, shaking well after each addition. The resulting suspension will contain cephalexin monohydrate equivalent to 125 mg cephalexin in each 5 mL (teaspoonful). 125 mg/5 mL (200 mL when mixed): Prepare suspension time at dispensing. Add to the bottle a total of 138 mL of water. For ease in preparation, tap bottle to loosen powder, add the water in 2 portions, shaking well after each addition. The resulting suspension will contain cephalexin monohydrate equivalent to 125 mg cephalexin in each 5 mL (teaspoonful). 250 mg/5 mL (100 mL when mixed): Prepare suspension time at dispensing. Add to the bottle a total of 69 mL of water. For ease in preparation, tap bottle to loosen powder, add the water in 2 portions, shaking well after each addition. The resulting suspension will contain cephalexin monohydrate equivalent to 250 mg cephalexin in each 5 mL (teaspoonful). 250 mg/5 mL (200 mL when mixed): Prepare suspension time at dispensing. Add to the bottle a total of 138 mL of water. For ease in preparation, tap bottle to loosen powder, add the water in 2 portions, shaking well after each addition. The resulting suspension will contain cephalexin monohydrate equivalent to 250 mg cephalexin in each 5 mL (teaspoonful). After mixing, the different concentrations and volumes of the suspension as described above, store in refrigerator. The suspension may be kept for 14 days without significant loss of potency.

Administer the following dosing regimens for cephalexin for oral suspension to patients with renal impairment [see Warnings and Precautions (5.4) and Use in Specific Populations (8.6)].

See Table 2 for the dosage in adults and pediatric patients at least 15 years of age with renal impairment.

Table 2. Recommended Cephalexin Dosage for Adult Patients and Pediatric Patients (at Least 15 Years of Age) with Renal Impairment

Renal function (Creatinine clearance)	Dosage recommendation
Greater than or equal to 60 mL/min	No dosage adjustment
30 mL/min to 59 mL/min	No dosage adjustment; maximum daily dose should not exceed 1 g
15 mL/min to 29 mL/min	250 mg, every 8 hours or every 12 hours
5 mL/min to 14 mL/min not yet on dialysis*	250 mg, every 24 hours
1 mL/min to 4 mL/min not yet on dialysis*	250 mg, every 48 hours or every 60 hours

^*There is insufficient information to make dose adjustment recommendations in patients on hemodialysis.

For oral suspension 125 mg/5mL and 250 mg/5mL of cephalexin as pink coloured powder for reconstitution in a multidose bottle that forms a pink coloured suspension with characteristic odour on constitution for each strength, respectively. For oral suspension: 125 mg/5mL and 250 mg/5mL of cephalexin as a powder in a multi-dose bottle for reconstitution (3)

Cephalexin is contraindicated in patients with known hypersensitivity to cephalexin or other members of the cephalosporin class of antibacterial drugs. Patients with known hypersensitivity to cephalexin or other members of the cephalosporin class of antibacterial drugs. (4)

Serious hypersensitivity (anaphylactic) reactions: Prior to use, inquire regarding history of hypersensitivity to beta-lactam antibacterial drugs. Discontinue the drug if signs or symptoms of an allergic reaction occur and institute supportive measures. (5.1) Clostridioides difficile -associated diarrhea (CDAD): Evaluate if diarrhea occurs. (5.2) Direct Coomb's Test Seroconversion: If anemia develops during or after cephalexin therapy, evaluate for drug-induced hemolytic anemia. (5.3) Seizure Potential: Use lower dose in patients with renal impairment. (5.4)

Allergic reactions in the form of rash, urticaria, angioedema, anaphylaxis, erythema multiforme, Stevens-Johnson syndrome, or toxic epidermal necrolysis have been reported with the use of cephalexin. Before therapy with cephalexin for oral suspension is instituted, inquire whether the patient has a history of hypersensitivity reactions to cephalexin, cephalosporins, penicillins, or other drugs. Cross-hypersensitivity among beta-lactam antibacterial drugs may occur in up to 10% of patients with a history of penicillin allergy. If an allergic reaction to cephalexin for oral suspension occurs, discontinue the drug and institute appropriate treatment.

Clostridioides difficile-associated diarrhea (CDAD) has been reported with use of nearly all antibacterial agents, including cephalexin, and may range in severity from mild diarrhea to fatal colitis. Treatment with antibacterial agents alters the normal flora of the colon leading to overgrowth of C. difficile. C. difficile produces toxins A and B, which contribute to the development of CDAD. Hypertoxin-producing strains of C. difficile cause increased morbidity and mortality, as these infections can be refractory to antimicrobial therapy and may require colectomy. CDAD must be considered in all patients who present with diarrhea following antibiotic use. Careful medical history is necessary since CDAD has been reported to occur over two months after the administration of antibacterial agents. If CDAD is suspected or confirmed, ongoing antibiotic use not directed against C. difficile may need to be discontinued. Appropriate fluid and electrolyte management, protein supplementation, antibiotic treatment of C. difficile, and surgical evaluation should be instituted as clinically indicated.

Positive direct Coombs' tests have been reported during treatment with the cephalosporin antibacterial drugs including cephalexin. Acute intravascular hemolysis induced by cephalexin therapy has been reported. If anemia develops during or after cephalexin therapy, perform a diagnostic work-up for drug-induced hemolytic anemia, discontinue cephalexin and institute appropriate therapy.

Several cephalosporins have been implicated in triggering seizures, particularly in patients with renal impairment when the dosage was not reduced. If seizures occur, discontinue cephalexin for oral suspension. Anticonvulsant therapy can be given if clinically indicated.

Cephalosporins may be associated with prolonged prothrombin time. Those at risk include patients with renal or hepatic impairment, or poor nutritional state, as well as patients receiving a protracted course of antibacterial therapy, and patients receiving anticoagulant therapy. Monitor prothrombin time in patients at risk and manage as indicated.

Prescribing cephalexin for oral suspension in the absence of a proven or strongly suspected bacterial infection is unlikely to provide benefit to the patient and increases the risk of the development of drug-resistant bacteria. Prolonged use of cephalexin for oral suspension may result in the overgrowth of nonsusceptible organisms. Careful observation of the patient is essential. If superinfection occurs during therapy, appropriate measures should be taken.

The following serious events are described in greater detail in the Warning and Precautions section: Hypersensitivity reactions [see Warning and Precautions (5.1)] Clostridioides difficile-associated diarrhea [see Warnings and Precautions (5.2)] Direct Coombs' Test Seroconversion [see Warnings and Precautions (5.3)] Seizure Potential [see Warnings and Precautions (5.4)] Prolonged Prothrombin Time [see Warnings and Precautions(5.5)] Development of Drug-Resistant Bacteria [see Warnings and Precautions(5.6)] The most common adverse reactions associated with cephalexin for oral suspension include diarrhea, nausea, vomiting, dyspepsia and abdominal pain. (6) To report SUSPECTED ADVERSE REACTIONS, contact Lupin Pharmaceuticals, Inc. at 1-800-399-2561 or to FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. 

Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. In clinical trials, the most frequent adverse reaction was diarrhea. Nausea and vomiting, dyspepsia, gastritis, and abdominal pain have also occurred. As with penicillins and other cephalosporins, transient hepatitis and cholestatic jaundice have been reported. Other reactions have included hypersensitivity reactions, genital and anal pruritus, genital candidiasis, vaginitis and vaginal discharge, dizziness, fatigue, headache, agitation, confusion, hallucinations, arthralgia, arthritis, and joint disorder. Reversible interstitial nephritis has been reported. Eosinophilia, neutropenia, thrombocytopenia, hemolytic anemia, and slight elevations in aspartate transaminase (AST) and alanine transaminase (ALT) have been reported. In addition to the adverse reactions listed above that have been observed in patients treated with cephalexin, the following adverse reactions and other altered laboratory tests have been reported for cephalosporin class antibacterial drugs: Other Adverse Reactions: Fever, colitis, aplastic anemia, hemorrhage, renal dysfunction, and toxic nephropathy. Altered Laboratory Tests: Prolonged prothrombin time, increased blood urea nitrogen (BUN), increased creatinine, elevated alkaline phosphatase, elevated bilirubin, elevated lactate dehydrogenase (LDH), pancytopenia, leukopenia, and agranulocytosis.

  Metformin: increased metformin concentrations. Monitor for hypoglycemia. (7.1)   Probenecid-The renal excretion of cephalexin for oral suspension is inhibited by probenecid. Co-administration of probenecid with cephalexin for oral suspension is not recommended. (7.2)   Administration of cephalexin for oral suspension may result in a false-positive reaction for glucose in the urine. (7.3)

Administration of cephalexin with metformin results in increased plasma metformin concentrations and decreased renal clearance of metformin. Careful patient monitoring and dose adjustment of metformin is recommended in patients concomitantly taking cephalexin and metformin [see Clinical Pharmacology (12.3)].

The renal excretion of cephalexin is inhibited by probenecid. Co-administration of probenecid with cephalexin is not recommended.

A false-positive reaction may occur when testing for the presence of glucose in the urine using Benedict's solution or Fehling's solution.

Renal Impairment: Monitor patients longer for toxicity and drug interactions due to delayed clearance. (8.6)

Risk Summary Available data from published epidemiologic studies and pharmacovigilance case reports over several decades of cephalexin use in pregnant women have not established drug-associated risks of major birth defects, miscarriage, or adverse maternal or fetal outcomes. Available studies have methodologic limitations, including small sample size, retrospective data collection, and inconsistent comparator groups. Animal reproduction studies with mice and rats using oral doses of cephalexin that are 0.6- and 1.2-times the maximum recommended human dose (MRHD) based on body surface area during organogenesis revealed no evidence of harm to the fetus (see Data). The background risk of major birth defects and miscarriage for the indicated population is unknown. All pregnancies have a background risk of birth defect, loss, or other adverse outcomes. In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2% to 4% and 15% to 20%, respectively. Data Animal Data In animal reproduction studies, pregnant mice and rats administered oral cephalexin doses of 250 or 500 mg/kg/day (approximately 0.6 and 1.2 times the MRHD) based on body surface area, respectively during the period of organogenesis showed no adverse effects on embryofetal development. In a pre- and post-natal developmental toxicity study, pregnant rats that received oral doses of 250 or 500 mg/kg/day of cephalexin from Day 15 of pregnancy to litter Day 21 showed no adverse effects on parturition, litter size, or growth of offspring.

Risk Summary Data from a published clinical lactation study report that cephalexin is present in human milk. The relative infant dose (RID) is considered to be <l% of the maternal weight adjusted dose. There are limited data on the effects of cephalexin on the breastfed child. There are no data on the effects of cephalexin on milk production. The developmental health benefits of breastfeeding should be considered along with the mother's clinical need for cephalexin and any potential adverse effects on the breastfed child from cephalexin or from the underlying maternal condition.

The safety and effectiveness of cephalexin have been established in pediatric patients aged one year and older in clinical trials [see Indications and Usage (1.1 – 1.5)] for the dosages described in the dosage and administration section [see Dosage and Administration (2.1, 2.2)]. The safety and effectiveness of cephalexin have not been established in pediatric patients younger than one year old.

Of the 701 subjects in 3 published clinical studies of cephalexin, 433 (62%) were 65 and over. No overall differences in safety or effectiveness were observed between these subjects and younger subjects, and other reported clinical experience has not identified differences in responses between the elderly and younger patients. This drug is substantially excreted by the kidney, and the risk of toxic reactions to this drug may be greater in patients with impaired renal function. Because elderly patients are more likely to have decreased renal function, care should be taken in dose selection [see Warnings and Precautions (5.4)].

Cephalexin should be administered with careful monitoring in the presence of renal impairment (creatinine clearance < 30 mL/min, with or without dialysis). Under such conditions, careful clinical observation and laboratory studies renal function monitoring should be conducted because safe dosage may be lower than that usually recommended [see Dosage and Administration (2.3)]. Monitor patients longer for toxicity and drug interactions due to delayed clearance.

Symptoms of oral overdose may include nausea, vomiting, epigastric distress, diarrhea, and hematuria. In the event of an overdose, institute general supportive measures. Forced diuresis, peritoneal dialysis, hemodialysis, or charcoal hemoperfusion have not been established as beneficial for an overdose of cephalexin.

Cephalexin for oral suspension, USP is a semisynthetic cephalosporin antibacterial drug intended for oral administration. It is 7- (D-α-Amino-α-phenylacetamido)-3-methyl-3-cephem-4-carboxylic acid monohydrate. Cephalexin has the molecular formula C16H17N3O4S • H2O and the molecular weight is 365.41. Cephalexin has the following structural formula: Cephalexin for oral suspension, USP is supplied in a multi-dose bottle as pink coloured powder containing 125 mg/5 mL or 250 mg/5 mL of cephalexin for oral use following reconstitution with water. Freshly reconstituted solutions of cephalexin yield a pink coloured suspension with characteristic odour on constitution for the 125 mg/5 mL and 250 mg/5 mL strengths, respectively. The inactive ingredients in the cephalexin for oral suspension are colloidal silicon dioxide, FD&C Red No. 40, sodium benzoate, strawberry flavor, sucrose, xanthan gum. Image 01

Cephalexin is a cephalosporin antibacterial drug [see Microbiology (12.4)].

Absorption: Cephalexin is acid stable and may be given without regard to meals. Following doses of 250 mg, 500 mg, and 1 g, average peak serum levels of approximately 9, 18, and 32 mcg/mL, respectively, were obtained at 1 hour. Serum levels were detectable 6 hours after administration (at a level of detection of 0.2 mcg/mL). Distribution: Cephalexin is approximately 10% to 15% bound to plasma proteins. Excretion: Cephalexin is excreted in the urine by glomerular filtration and tubular secretion. Studies showed that over 90% of the drug was excreted unchanged in the urine within 8 hours. During this period, peak urine concentrations following the 250 mg, 500 mg, and 1 g doses were approximately 1000, 2200, and 5000 mcg/mL respectively. Drug Interactions: In healthy subjects given single 500 mg doses of cephalexin and metformin, plasma metformin mean Cmax and AUC increased by an average of 34% and 24%, respectively, and metformin mean renal clearance decreased by 14%. No information is available about the interaction of cephalexin and metformin following multiple doses of either drug.

Mechanism of Action  Cephalexin is a bactericidal agent that acts by the inhibition of bacterial cell-wall synthesis. Resistance Methicillin-resistant staphylococci and most isolates of enterococci are resistant to cephalexin. Cephalexin is not active against most isolates of Enterobacter spp., Morganella morganii, and Proteus vulgaris. Cephalexin has no activity against Pseudomonas spp., or Acinetobacter calcoaceticus. Penicillin-resistant Streptococcus pneumoniae is usually cross-resistant to beta-lactam antibacterial drugs. Antimicrobial Activity Cephalexin has been shown to be active against most isolates of the following bacteria both in vitro and in clinical infections [see Indications and Usage (1)]. Gram-positive bacteria Staphylococcus aureus (methicillin-susceptible isolates only) Streptococcus pneumoniae (penicillin-susceptible isolates) Streptococcus pyogenes Gram-negative bacteria Escherichia coli Haemophilus influenzae Klebsiella pneumoniae Moraxella catarrhalis Proteus mirabilis Susceptibility Testing For specific information regarding susceptibility test interpretive criteria and associated test methods and quality control standards recognized by FDA for this drug, please see: https://www.fda.gov/STIC.

Lifetime studies in animals have not been performed to evaluate the carcinogenic potential of cephalexin. Tests to determine the mutagenic potential of cephalexin have not been performed. In male and female rats, fertility and reproductive performance were not affected by cephalexin oral doses up to 1.5 times the highest recommended human dose based upon body surface area.

Cephalexin for Oral Suspension USP is a Pink coloured powder forming pink coloured suspension with characteristic odour on constitution for the 125mg/5mL and 250mg/5mL strength, respectively, supplied as follows: The 125 mg per 5 mL for oral suspension is available as follows: 100-mL Bottles                 NDC 68180-440-01 200-mL Bottles                 NDC 68180-440-02 The 250 mg per 5 mL for oral suspension is available as follows: 100-mL Bottles NDC 68180-441-01 200-mL Bottles NDC 68180-441-02 Directions for mixing are included elsewhere in the labeling [see Dosage and Administration (2.3)]. Prior to mixing, store at 20°C to 25°C (68°F to 77°F) [See USP Controlled Room Temperature]. Shake well before using. Keep tightly closed. After mixing, store in refrigerator. May be kept for 14 days without significant loss of potency[see Dosage and Administration (2.3)].

Allergic Reactions Advise patients that allergic reactions, including serious allergic reactions, could occur and that serious reactions require immediate treatment. Ask the patient about any previous hypersensitivity reactions to cephalexin, other beta-lactams (including cephalosporins) or other allergens (5.1) Diarrhea Advise patients that diarrhea is a common problem caused by antibacterial drugs and usually resolves when the drug is discontinued. Sometimes, frequent watery or bloody diarrhea may occur and may be a sign of a more serious intestinal infection. If severe watery or bloody diarrhea develops, advise patients to contact their healthcare provider. Antibacterial Resistance Patients should be counseled that antibacterial drugs including cephalexin, should only be used to treat bacterial infections. They do not treat viral infections (e.g., the common cold). When cephalexin is prescribed to treat a bacterial infection, tell patients that although it is common to feel better early in the course of therapy, the medication should be taken exactly as directed. Skipping doses or not completing the full course of therapy may (1) decrease the effectiveness of the immediate treatment and (2) increase the likelihood that bacteria will develop resistance and will not be treatable by cephalexin or other antibacterial drugs in the future. Manufactured for: Lupin Pharmaceuticals, Inc. Naples, FL 34108 United States Manufactured by: Lupin Limited Mandideep 462046 India Revised: May 2026                                                                              ID: 284100 Image 02

CEPHALEXIN FOR ORAL SUSPENSION USP Rx Only 125 mg/5 mL NDC 68180-440-01 100 mL Bottles CEPHALEXIN FOR ORAL SUSPENSION USP Rx Only 250 mg/5 mL NDC 68180-441-01 100 mL Bottles CEPHALEXIN FOR ORAL SUSPENSION USP Rx Only 125 mg/5 mL NDC 68180-440-02 200 mL Bottles CEPHALEXIN FOR ORAL SUSPENSION USP Rx Only 250 mg/5 mL NDC 68180-441-02 200 mL Bottles Image 03 Image 04 Image 05 Image 06