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 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: | Glenmark Pharmaceuticals Inc., USA |
NON-PROPRIETARY NAME: | Norethindrone Acetate and Ethinyl Estradiol |
SUBSTANCE NAME: | NORETHINDRONE ACETATE; ETHINYL ESTRADIOL |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Estrogen [EPC],Estrogen Receptor Agonists [MoA],Progesterone Congeners [Chemical/Ingredient],Progestin [EPC] |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2015-04-02 |
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: | .5; 2.5(mg/1; ug/1) |
START MARKETING DATE: | 2015-04-02 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 68462-656_cf549b5a-2707-4020-9f94-dab1260e1664 |
PRODUCT NDC: | 68462-656 |
APPLICATION NUMBER: | ANDA203038 |
Other NORETHINDRONE ACETATE; ETHINYL ESTRADIOL Pharmaceutical Manufacturers / Labelers: