Dutasteride
- Product NDC
- 70518-1966
- 11-digit product format
- 705181966
- Labeler code
- 70518
- Product ID
- 70518-1966_848f0b68-e6df-637f-e053-2991aa0a118f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dutasteride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA203118
- Marketing category
- ANDA
- Marketing start
- 2019-03-19
- 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