Dutasteride
- Product NDC
- 60429-935
- 11-digit product format
- 604290935
- Labeler code
- 60429
- Product ID
- 60429-935_a038aa4f-d5cd-0368-e053-2a95a90a8b78
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- dutasteride
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Golden State Medical Supply
- Application
- ANDA204292
- Marketing category
- ANDA
- Marketing start
- 2015-11-24
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record