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 57237-062
Finasteride 5 mg tablet, film coated
On the label: Rising Pharma Holdings, Inc..
Where it's made
Product details
- Generic drug
- Finasteride: see every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 5 mg
- Approval
- ANDA ANDA078341
- On the market since
- Oct 30, 2007
- Package NDCs
57237-062-0557237-062-3057237-062-90- Official label
- DailyMed (National Library of Medicine), updated Aug 17, 2026
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