NDC 76519-1172
Cefdinir 125 mg per 5 mL powder, for suspension
On the label: H.J. Harkins Co., Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| H.J. Harkins Company, Inc. | Grover Beach, California, United States | Makes it, repackages it and relabels it | Problems found, fixed voluntarilyMar 3, 2023 · 5 inspections |
Product details
- Generic drug
- Cefdinir: every company that makes it
- Form
- powder, for suspension
- Strength
- 125 mg per 5 mL
- Approval
- ANDA ANDA065332
- On the market since
- Mar 26, 2018
- Package NDCs
76519-1172-6- Official label
- DailyMed (National Library of Medicine), updated Sep 19, 2018
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