NDC 59651-322
Cephalexin 125 mg per 5 mL powder, for suspension
On the label: Aurobindo Pharma Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Sangareddy, India | Makes it and tests it | Problems found, fixed voluntarilySep 29, 2023 · 5 inspections, 1 with FDA action |
Product details
- Generic drug
- Cephalexin: every company that makes it
- Form
- powder, for suspension, oral
- Strength
- 125 mg per 5 mL
- Approval
- ANDA ANDA213568
- On the market since
- Jun 9, 2026
- Package NDCs
59651-322-0159651-322-02- Official label
- DailyMed (National Library of Medicine), updated Jul 21, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?