bexarotene
- Product NDC
- 68682-002
- 11-digit product format
- 686820002
- Labeler code
- 68682
- Product ID
- 68682-002_edd0c9df-745b-4e32-a0a5-959d414f7547
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bexarotene
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Oceanside Pharmaceuticals
- Application
- NDA021056
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2000-06-28
- Marketing end
- 0000-00-00
- Substance
- BEXAROTENE
- Active strength
- 1 g/100g
- 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 |
|---|
| 68682-002-60 | 68682000260 | 60 g in 1 TUBE (68682-002-60) | 60 g | 2022-05-13 | 0000-00-00 | No | No | Current |