NDC 68682-002
bexarotene
Bexarotene
bexarotene is a Topical Gel in the Human Prescription Drug category. It is labeled and distributed by Oceanside Pharmaceuticals. The primary component is Bexarotene.
| Product ID | 68682-002_36e82a97-571f-48f2-bb36-7313aa7e01f3 |
| NDC | 68682-002 |
| Product Type | Human Prescription Drug |
| Proprietary Name | bexarotene |
| Generic Name | Bexarotene |
| Dosage Form | Gel |
| Route of Administration | TOPICAL |
| Marketing Start Date | 2000-06-28 |
| Marketing Category | NDA AUTHORIZED GENERIC / |
| Application Number | NDA021056 |
| Labeler Name | Oceanside Pharmaceuticals |
| Substance Name | BEXAROTENE |
| Active Ingredient Strength | 1 g/100g |
| Pharm Classes | Retinoid [EPC], Retinoids [CS] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2023-12-31 |