NDC 54868-4120
Propecia 1 mg tablet, film coated
On the label: Physicians Total Care, Inc.. It's repackaged from NDC 0006-0071, made by Merck Sharp & Dohme Corp. (Propecia). 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 Physicians Total Care, Inc. names for other drugs.
Product details
- Generic drug
- Finasteride: every company that makes it
- Form
- tablet, film coated
- Strength
- 1 mg
- Approval
- NDA NDA020788
- On the market since
- Dec 19, 1997
- Package NDCs
54868-4120-054868-4120-1- Official label
- DailyMed (National Library of Medicine), updated Jun 11, 2013
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?