Tretinoin
- Product NDC
- 63629-2285
- 11-digit product format
- 636292285
- Labeler code
- 63629
- Product ID
- 63629-2285_4dea2e94-1ff3-4eeb-ab1f-bb4a0e0a9cd1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tretinoin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA201687
- Marketing category
- ANDA
- Marketing start
- 2012-10-24
- Marketing end
- 0000-00-00
- Substance
- TRETINOIN
- Active strength
- 10 mg/1
- Pharmacologic classes
- Retinoid [EPC], Retinoids [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 63629-2285-1 | 63629228501 | 100 CAPSULE in 1 BOTTLE (63629-2285-1) | 100 capsule | 2021-03-29 | 0000-00-00 | No | No | Current |