bexarotene (Oceanside Pharmaceuticals)
Welcome to the PulseAid listing for the bexarotene drug offered from Oceanside Pharmaceuticals. This Retinoid [EPC],Retinoids [Chemical/Ingredient] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
| LABELER NAME / MANUFACTURER: | Oceanside Pharmaceuticals |
| NON-PROPRIETARY NAME: | bexarotene |
| SUBSTANCE NAME: | BEXAROTENE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Retinoid [EPC],Retinoids [Chemical/Ingredient] |
| ROUTE: | ORAL |
| DOSAGE FORM: | CAPSULE, LIQUID FILLED |
| MARKETING CATEGORY NAME: | NDA AUTHORIZED GENERIC |
| START MARKETING DATE: | 2015-12-17 |
| END MARKETING DATE: | 0000-00-00 |
bexarotene HUMAN PRESCRIPTION DRUG Details:
| Item Description | bexarotene from Oceanside Pharmaceuticals |
| LABELER NAME: | Oceanside Pharmaceuticals |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 75(mg/1) |
| START MARKETING DATE: | 2015-12-17 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 68682-003_8f5964b7-0df5-4f2a-b6db-4a055c64d902 |
| PRODUCT NDC: | 68682-003 |
| APPLICATION NUMBER: | NDA021055 |
Other BEXAROTENE Pharmaceutical Manufacturers / Labelers:
