FABIOR (Mayne Pharma LLC)


Welcome to the PulseAid listing for the FABIOR drug offered from Mayne Pharma LLC. 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: Mayne Pharma LLC
NON-PROPRIETARY NAME: tazarotene
SUBSTANCE NAME: TAZAROTENE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Retinoid [EPC],Retinoids [Chemical/Ingredient]
ROUTE: TOPICAL
DOSAGE FORM: AEROSOL, FOAM
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2017-03-10
END MARKETING DATE: 0000-00-00


FABIOR HUMAN PRESCRIPTION DRUG Details:

Item DescriptionFABIOR from Mayne Pharma LLC
LABELER NAME: Mayne Pharma LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 1(mg/g)
START MARKETING DATE: 2017-03-10
END MARKETING DATE: 0000-00-00
PRODUCT ID: 51862-295_36320220-2d8d-4854-84a4-924ae33ffb81
PRODUCT NDC: 51862-295
APPLICATION NUMBER: NDA202428

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