NDC 71335-1836
terbinafine hydrochloride 250 mg tablet
On the label: Bryant Ranch Prepack. It's repackaged from NDC 42043-410, made by OrchidPharma 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 repackages it and 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 Bryant Ranch Prepack names for other drugs.
Product details
- Generic drug
- Terbinafine: every company that makes it
- Form
- tablet
- Strength
- 250 mg
- Approval
- ANDA ANDA078163
- On the market since
- Oct 1, 2020
- Package NDCs
71335-1836-171335-1836-271335-1836-371335-1836-471335-1836-571335-1836-671335-1836-771335-1836-871335-1836-9- Official label
- DailyMed (National Library of Medicine), updated Nov 30, 2023
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?