Bexarotene
- Product NDC
- 0054-0399
- 11-digit product format
- 000540399
- Labeler code
- 0054
- Product ID
- 0054-0399_2be86673-4c9c-4543-a545-9871a8f72e12
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bexarotene
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Application
- ANDA203663
- Marketing category
- ANDA
- Marketing start
- 2020-11-11
- Marketing end
- 0000-00-00
- Substance
- BEXAROTENE
- Active strength
- 75 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0054-0399-25 | 00054039925 | 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (0054-0399-25) | 2020-11-11 | 0000-00-00 | No | No | Current |