NDC 0591-2832
bexarotene
Bexarotene
bexarotene is a Oral Capsule, Liquid Filled in the Human Prescription Drug category. It is labeled and distributed by Actavis Pharma, Inc.. The primary component is Bexarotene.
| Product ID | 0591-2832_66571927-4b7a-4141-9d0b-05aafb9b5db6 |
| NDC | 0591-2832 |
| Product Type | Human Prescription Drug |
| Proprietary Name | bexarotene |
| Generic Name | Bexarotene |
| Dosage Form | Capsule, Liquid Filled |
| Route of Administration | ORAL |
| Marketing Start Date | 2021-11-11 |
| Marketing Category | ANDA / |
| Application Number | ANDA209931 |
| Labeler Name | Actavis Pharma, Inc. |
| Substance Name | BEXAROTENE |
| Active Ingredient Strength | 75 mg/1 |
| Pharm Classes | Retinoid [EPC], Retinoids [CS] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2023-12-31 |