Nortrel21 Day (Teva Pharmaceuticals USA, Inc.)
Welcome to the PulseAid listing for the Nortrel drug offered from Teva Pharmaceuticals USA, Inc.. This Progesterone Congeners [Chemical/Ingredient],Progestin [EPC],Estrogen [EPC],Estrogen Receptor Agonists [MoA] 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: | Norethindrone and Ethinyl Estradiol |
| SUBSTANCE NAME: | NORETHINDRONE; ETHINYL ESTRADIOL |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Progesterone Congeners [Chemical/Ingredient],Progestin [EPC],Estrogen [EPC],Estrogen Receptor Agonists [MoA] |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2001-06-13 |
| END MARKETING DATE: | 0000-00-00 |
Nortrel 21 Day HUMAN PRESCRIPTION DRUG Details:
| Item Description | Nortrel 21 Day from Teva Pharmaceuticals USA, Inc. |
| LABELER NAME: | Teva Pharmaceuticals USA, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 1; .035(mg/1; mg/1) |
| START MARKETING DATE: | 2001-06-13 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0555-9009_3ca5a20b-8b30-4ed8-b668-617b250e41fc |
| PRODUCT NDC: | 0555-9009 |
| APPLICATION NUMBER: | ANDA072693 |
Other NORETHINDRONE; ETHINYL ESTRADIOL Pharmaceutical Manufacturers / Labelers:
