NDC 68071-2381
Terbinafine Hydrochloride 250 mg tablet
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Cipla USA., Inc.'s NDC 69097-731.
Where the pills inside were made
This label doesn't name the factory that makes the drug. 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 Cipla USA., Inc. names for other drugs.
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · relabels it
Product details
- Generic drug
- Terbinafine: every company that makes it
- Form
- tablet, oral
- Strength
- 250 mg
- Approval
- ANDA ANDA077137
- On the market since
- Jan 8, 2021
- Package NDCs
68071-2381-3- Official label
- DailyMed (National Library of Medicine), updated Mar 2, 2026
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