Dutasteride
- Product NDC
- 70518-2256
- 11-digit product format
- 705182256
- Labeler code
- 70518
- Product ID
- 70518-2256_8fe089b4-50de-2c24-e053-2995a90a5202
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dutasteride
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA204262
- Marketing category
- ANDA
- Marketing start
- 2019-08-07
- 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