Estropipate (Actavis Pharma, Inc.)
Welcome to the PulseAid listing for the Estropipate drug offered from Actavis Pharma, Inc.. This 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: | Actavis Pharma, Inc. |
| NON-PROPRIETARY NAME: | Estropipate |
| SUBSTANCE NAME: | ESTROPIPATE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 1993-09-23 |
| END MARKETING DATE: | 0000-00-00 |
Estropipate HUMAN PRESCRIPTION DRUG Details:
| Item Description | Estropipate from Actavis Pharma, Inc. |
| LABELER NAME: | Actavis Pharma, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 0.75(mg/1) |
| START MARKETING DATE: | 1993-09-23 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0591-0414_0cd4e8ed-b807-47d4-9926-d22d80ff1c33 |
| PRODUCT NDC: | 0591-0414 |
| APPLICATION NUMBER: | ANDA081213 |
Other ESTROPIPATE Pharmaceutical Manufacturers / Labelers:
