NDC 68071-1640
Terbinafine Hydrochloride 250 mg tablet
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged from NDC 67405-500, made by Harris Pharmaceutical, Inc. (Terbinafine Hydrochloride). 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
- Terbinafine: every company that makes it
- Form
- tablet, oral
- Strength
- 250 mg
- Approval
- ANDA ANDA077137
- On the market since
- Aug 13, 2014
- Package NDCs
68071-1640-3- Official label
- DailyMed (National Library of Medicine), updated Jul 15, 2024
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