Cephalexin 59651-0322
Product NDC
59651-0322- Manufacturer
- Aurobindo Pharma Limited
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 9, 2026
- Listing Expires
- December 31, 2027
- Application
- ANDA213568
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Cephalexin | 125 mg/5mL |
Drug Class
Cephalosporin Antibacterial [EPC]Cephalosporins [CS]
Packaging Options(2)
100 mL in 1 BOTTLE (59651-322-01)
200 mL in 1 BOTTLE (59651-322-02)