Bexarotene (Mylan Institutional Inc.)


Welcome to the PulseAid listing for the Bexarotene drug offered from Mylan Institutional 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 Institutional 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: 2016-04-15
END MARKETING DATE: 0000-00-00


Bexarotene HUMAN PRESCRIPTION DRUG Details:

Item DescriptionBexarotene from Mylan Institutional Inc.
LABELER NAME: Mylan Institutional Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 75(mg/1)
START MARKETING DATE: 2016-04-15
END MARKETING DATE: 0000-00-00
PRODUCT ID: 42292-007_9410215d-828c-454c-a44e-ad0fb0c65f68
PRODUCT NDC: 42292-007
APPLICATION NUMBER: ANDA203174

Other BEXAROTENE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Mylan Institutional Inc.Bexarotene
Mylan Pharmaceuticals Inc.Bexarotene
Oceanside Pharmaceuticalsbexarotene
Valeant Pharmaceuticals North America LLCTargretin