Dutasteride
- Product NDC
- 50268-282
- 11-digit product format
- 502680282
- Labeler code
- 50268
- Product ID
- 50268-282_6593de91-905c-e547-e053-2991aa0ad131
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dutasteride
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- AvPAK
- Application
- ANDA206574
- Marketing category
- ANDA
- Marketing start
- 2017-11-07
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50268-282-13 | 50268028213 | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-282-13) > 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (50268-282-11) | 30 blister pack | 2017-11-07 | 0000-00-00 | No | No | Current |