NDC 24979-155
Cephalexin 250 mg per 5 mL powder, for suspension
On the label: TWi Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Yung Shin Pharm. Ind. Co., Ltd. | Taichung City, Taiwan | Makes it, tests it and packages it | Problems found, fixed voluntarilyOct 22, 2019 · 7 inspections, 1 with FDA action |
Product details
- Generic drug
- Cephalexin: every company that makes it
- Form
- powder, for suspension
- Strength
- 250 mg per 5 mL
- Approval
- ANDA ANDA065336
- On the market since
- Feb 28, 2018
- Package NDCs
24979-155-1424979-155-38- Official label
- DailyMed (National Library of Medicine), updated Aug 20, 2019
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