Aurobindo Pharma Limited
Medchal, India · makes it and tests it
Problems found, fixed voluntarily Last FDA inspection Jul 21, 2023. 13 inspections on record, 1 with serious problems.
NDC 50436-0927
Finasteride 1 mg tablet, film coated
On the label: Unit Dose Services.
It's a repackaged product: Unit Dose Services rebottles it from Aurobindo Pharma Limited's NDC 65862-927.
Where the pills inside were made
Repackaging site
- Unit Dose Services, · repackages it and relabels it
Product details
- Generic drug
- Finasteride: see every company that makes it
- Form
- tablet, film coated
- Strength
- 1 mg
- Approval
- ANDA ANDA203687
- On the market since
- Sep 20, 2014
- Package NDCs
50436-0927-150436-0927-3- Official label
- DailyMed (National Library of Medicine), updated Dec 6, 2018
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?