Tazarotene (Taro Pharmaceuticals U.S.A., Inc.)


Welcome to the PulseAid listing for the Tazarotene drug offered from Taro Pharmaceuticals U.S.A., 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: Taro Pharmaceuticals U.S.A., Inc.
NON-PROPRIETARY NAME: Tazarotene
SUBSTANCE NAME: TAZAROTENE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Retinoid [EPC],Retinoids [Chemical/Ingredient]
ROUTE: TOPICAL
DOSAGE FORM: CREAM
MARKETING CATEGORY NAME: ANDA
START MARKETING DATE: 2017-04-03
END MARKETING DATE: 0000-00-00


Tazarotene HUMAN PRESCRIPTION DRUG Details:

Item DescriptionTazarotene from Taro Pharmaceuticals U.S.A., Inc.
LABELER NAME: Taro Pharmaceuticals U.S.A., Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 1(mg/g)
START MARKETING DATE: 2017-04-03
END MARKETING DATE: 0000-00-00
PRODUCT ID: 51672-1373_423e1f72-7ad6-4982-946d-197cb19a3b22
PRODUCT NDC: 51672-1373
APPLICATION NUMBER: ANDA208258

Other TAZAROTENE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Allergan, Inc.TAZORAC
Mayne Pharma LLCFABIOR
Pacific Pharma, Inc.Tazarotene
Physicians Total Care, Inc.Tazorac
Stiefel Laboratories, Inc.Fabior
Taro Pharmaceuticals U.S.A., Inc.Tazarotene