bexarotene
- Product NDC
- 68682-003
- 11-digit product format
- 686820003
- Labeler code
- 68682
- Product ID
- 68682-003_22590cf5-85a5-4129-a313-2e1cb2aba25d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bexarotene
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Oceanside Pharmaceuticals
- Application
- NDA021055
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2015-12-17
- 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
- 2021-12-31
- 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 |
|---|
| 68682-003-10 | 68682000310 | 1 BOTTLE in 1 CARTON (68682-003-10) > 100 CAPSULE, LIQUID FILLED in 1 BOTTLE | 1 bottle | 2015-12-17 | 0000-00-00 | No | No | Current |