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 76420-151
Finasteride 1 mg tablet, film coated
On the label: Asclemed USA, Inc..
It's a repackaged product: Asclemed USA, Inc. rebottles it from Rising Pharma Holdings, Inc.'s NDC 57237-061.
Where the pills inside were made
Repackaging site
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · relabels it
Product details
- Generic drug
- Finasteride: see every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 1 mg
- Approval
- ANDA ANDA203687
- On the market since
- Nov 5, 2013
- Package NDCs
76420-151-3076420-151-90- Official label
- DailyMed (National Library of Medicine), updated Jan 17, 2022
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