Norethindrone Acetate and Ethinyl Estradiol (Glenmark Pharmaceuticals Inc., USA)
Welcome to the PulseAid listing for the Norethindrone Acetate and Ethinyl Estradiol drug offered from Glenmark Pharmaceuticals Inc., USA. 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: | Glenmark Pharmaceuticals Inc., USA |
NON-PROPRIETARY NAME: | Norethindrone Acetate and Ethinyl Estradiol |
SUBSTANCE NAME: | NORETHINDRONE ACETATE; 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: | 2016-01-20 |
END MARKETING DATE: | 0000-00-00 |
Norethindrone Acetate and Ethinyl Estradiol HUMAN PRESCRIPTION DRUG Details:
Item Description | Norethindrone Acetate and Ethinyl Estradiol from Glenmark Pharmaceuticals Inc., USA |
LABELER NAME: | Glenmark Pharmaceuticals Inc., USA |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 1; .02(mg/1; mg/1) |
START MARKETING DATE: | 2016-01-20 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 68462-132_94c51903-5fe8-4c7b-a746-e08f231dce89 |
PRODUCT NDC: | 68462-132 |
APPLICATION NUMBER: | ANDA206969 |
Other NORETHINDRONE ACETATE; ETHINYL ESTRADIOL Pharmaceutical Manufacturers / Labelers: