Bexarotene (Mylan Pharmaceuticals Inc.)
Welcome to the PulseAid listing for the Bexarotene drug offered from Mylan Pharmaceuticals Inc.. 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: | Mylan Pharmaceuticals Inc. |
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: | ANDA |
START MARKETING DATE: | 2015-07-09 |
END MARKETING DATE: | 0000-00-00 |
Bexarotene HUMAN PRESCRIPTION DRUG Details:
Item Description | Bexarotene from Mylan Pharmaceuticals Inc. |
LABELER NAME: | Mylan Pharmaceuticals Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 75(mg/1) |
START MARKETING DATE: | 2015-07-09 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0378-6955_2d1eb4bd-51f9-4c9b-9fb1-0be5e30a3dc5 |
PRODUCT NDC: | 0378-6955 |
APPLICATION NUMBER: | ANDA203174 |
Other BEXAROTENE Pharmaceutical Manufacturers / Labelers: