NDC 64725-1438
Fluphenazine Hydrochloride 5 mg tablet, film coated
On the label: TYA Pharmaceuticals. It's repackaged from NDC 0781-1438, made by Sandoz Inc (Fluphenazine 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 TYA Pharmaceuticals names for other drugs.
Product details
- Generic drug
- Fluphenazine: every company that makes it
- Form
- tablet, film coated
- Strength
- 5 mg
- Approval
- ANDA ANDA089586
- On the market since
- Oct 16, 1987
- Package NDCs
64725-1438-1- Official label
- DailyMed (National Library of Medicine), updated Oct 14, 2013
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?