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 Description | Danazol from Teva Pharmaceuticals USA, Inc. |
LABELER NAME: | Teva Pharmaceuticals USA, Inc. |
DEA SCHEDULE: |
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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: