Danazol (Teva Pharmaceuticals USA, Inc.)


Welcome to the PulseAid listing for the Danazol drug offered from Teva Pharmaceuticals USA, Inc.. This Androgen [EPC],Androgen Receptor Agonists [MoA],Androstanes [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: Teva Pharmaceuticals USA, Inc.
NON-PROPRIETARY NAME: Danazol
SUBSTANCE NAME: DANAZOL
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Androgen [EPC],Androgen Receptor Agonists [MoA],Androstanes [Chemical/Ingredient]
ROUTE: ORAL
DOSAGE FORM: CAPSULE
MARKETING CATEGORY NAME: ANDA
START MARKETING DATE: 1998-06-25
END MARKETING DATE: 0000-00-00


Danazol HUMAN PRESCRIPTION DRUG Details:

Item DescriptionDanazol from Teva Pharmaceuticals USA, Inc.
LABELER NAME: Teva Pharmaceuticals USA, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 50(mg/1)
START MARKETING DATE: 1998-06-25
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0555-0633_4eb76ac7-9ce0-43aa-bc8e-06e6b7dafea4
PRODUCT NDC: 0555-0633
APPLICATION NUMBER: ANDA074582

Other DANAZOL Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
AvKARE, Inc.Danazol
Carilion Materials ManagementDanazol
Lannett Company, Inc.Danazol
Teva Pharmaceuticals USA, Inc.Danazol