Estradiol / Norethindrone Acetate (Breckenridge Pharmaceutical, Inc.)
Welcome to the PulseAid listing for the Estradiol / Norethindrone Acetate drug offered from Breckenridge Pharmaceutical, Inc.. This Estradiol Congeners [Chemical/Ingredient],Estrogen [EPC],Estrogen Receptor Agonists [MoA],Progesterone Congeners [Chemical/Ingredient],Progestin [EPC] 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: | Breckenridge Pharmaceutical, Inc. |
| NON-PROPRIETARY NAME: | Estradiol and Norethindrone Acetate |
| SUBSTANCE NAME: | ESTRADIOL; NORETHINDRONE ACETATE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Estradiol Congeners [Chemical/Ingredient],Estrogen [EPC],Estrogen Receptor Agonists [MoA],Progesterone Congeners [Chemical/Ingredient],Progestin [EPC] |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET, FILM COATED |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2008-04-17 |
| END MARKETING DATE: | 0000-00-00 |
Estradiol / Norethindrone Acetate HUMAN PRESCRIPTION DRUG Details:
| Item Description | Estradiol / Norethindrone Acetate from Breckenridge Pharmaceutical, Inc. |
| LABELER NAME: | Breckenridge Pharmaceutical, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 1; .5(mg/1; mg/1) |
| START MARKETING DATE: | 2008-04-17 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 51991-474_2caec137-d8d4-4a0a-a193-b3877c39bb34 |
| PRODUCT NDC: | 51991-474 |
| APPLICATION NUMBER: | ANDA078324 |
Other ESTRADIOL; NORETHINDRONE ACETATE Pharmaceutical Manufacturers / Labelers:
