Dutasteride
- Product NDC
- 68071-4237
- 11-digit product format
- 680714237
- Labeler code
- 68071
- Product ID
- 68071-4237_630fec2e-30e8-3c1b-e053-2a91aa0aba11
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- dutasteride
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA204292
- Marketing category
- ANDA
- Marketing start
- 2015-11-25
- Marketing end
- 0000-00-00
- Substance
- DUTASTERIDE
- Active strength
- 1 mg/1
- Pharmacologic classes
- 5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record