Dutasteride
- Product NDC
- 63187-657
- 11-digit product format
- 631870657
- Labeler code
- 63187
- Product ID
- 63187-657_87202048-a4a1-47e3-9dad-fb99caea07fb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dutasteride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA202808
- Marketing category
- ANDA
- Marketing start
- 2015-11-20
- 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