NDC 68071-1645
Cefdinir 250 mg per 5 mL powder, for suspension
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged from NDC 16714-393, made by NorthStar Rx LLC (Cefdinir). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 1 site that relabels it). Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants NuCare Pharmaceuticals.Inc. names for other drugs.
Product details
- Generic drug
- Cefdinir: every company that makes it
- Form
- powder, for suspension
- Strength
- 250 mg per 5 mL
- Approval
- ANDA ANDA065473
- On the market since
- Dec 14, 2007
- Package NDCs
68071-1645-1- Official label
- DailyMed (National Library of Medicine), updated Jan 13, 2022
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