AZELEX (Allergan, Inc.)


Welcome to the PulseAid listing for the AZELEX drug offered from Allergan, Inc.. This Decreased Protein Synthesis [PE],Decreased Sebaceous Gland Activity [PE] 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: Allergan, Inc.
NON-PROPRIETARY NAME: azelaic acid
SUBSTANCE NAME: AZELAIC ACID
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Decreased Protein Synthesis [PE],Decreased Sebaceous Gland Activity [PE]
ROUTE: CUTANEOUS
DOSAGE FORM: CREAM
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 1996-03-21
END MARKETING DATE: 0000-00-00


AZELEX HUMAN PRESCRIPTION DRUG Details:

Item DescriptionAZELEX from Allergan, Inc.
LABELER NAME: Allergan, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 0.2(g/g)
START MARKETING DATE: 1996-03-21
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0023-8694_d7a96fba-04c1-4af1-9e4b-6e22d4e1fdd0
PRODUCT NDC: 0023-8694
APPLICATION NUMBER: NDA020428

Other AZELAIC ACID Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Allergan, Inc.AZELEX
Alvogen, Inc.Azelaic Acid
Bayer HealthCare Pharmaceuticals Inc.Finacea
Intendis Inc.Finacea
Physicians Total Care, Inc.Finacea