Premarin (Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer Inc.)
Welcome to the PulseAid listing for the Premarin drug offered from Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer Inc.. This Estrogen [EPC],Estrogen Receptor Agonists [MoA],Estrogens, Conjugated (USP) [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: | Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer Inc. |
| NON-PROPRIETARY NAME: | conjugated estrogens |
| SUBSTANCE NAME: | ESTROGENS, CONJUGATED |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Estrogen [EPC],Estrogen Receptor Agonists [MoA],Estrogens, Conjugated (USP) [Chemical/Ingredient] |
| ROUTE: | INTRAMUSCULAR; INTRAVENOUS |
| DOSAGE FORM: | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 1956-12-01 |
| END MARKETING DATE: | 0000-00-00 |
Premarin HUMAN PRESCRIPTION DRUG Details:
| Item Description | Premarin from Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer Inc. |
| LABELER NAME: | Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 25(mg/5mL) |
| START MARKETING DATE: | 1956-12-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0046-0749_eaad8e44-f510-4b8c-a5da-c6f0cd29b466 |
| PRODUCT NDC: | 0046-0749 |
| APPLICATION NUMBER: | NDA010402 |
Other ESTROGENS, CONJUGATED Pharmaceutical Manufacturers / Labelers:
