Levonorgestrel and Ethinyl Estradiol (Glenmark Pharmaceuticals Inc., USA)
Welcome to the PulseAid listing for the Levonorgestrel and Ethinyl Estradiol drug offered from Glenmark Pharmaceuticals Inc., USA. This Inhibit Ovum Fertilization [PE],Progesterone Congeners [Chemical/Ingredient],Progesterone Congeners [Chemical/Ingredient],Progestin [EPC],Progestin-containing Intrauterine Device [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: | Levonorgestrel and Ethinyl Estradiol |
SUBSTANCE NAME: | LEVONORGESTREL; ETHINYL ESTRADIOL |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Inhibit Ovum Fertilization [PE],Progesterone Congeners [Chemical/Ingredient],Progesterone Congeners [Chemical/Ingredient],Progestin [EPC],Progestin-containing Intrauterine Device [EPC],Estrogen [EPC],Estrogen Receptor Agonists [MoA] |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2015-04-09 |
END MARKETING DATE: | 0000-00-00 |
Levonorgestrel and Ethinyl Estradiol HUMAN PRESCRIPTION DRUG Details:
Item Description | Levonorgestrel and Ethinyl Estradiol from Glenmark Pharmaceuticals Inc., USA |
LABELER NAME: | Glenmark Pharmaceuticals Inc., USA |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 90; 20(ug/1; ug/1) |
START MARKETING DATE: | 2015-04-09 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 68462-637_33a3a210-87b7-4064-9e3c-70c50484478a |
PRODUCT NDC: | 68462-637 |
APPLICATION NUMBER: | ANDA202791 |
Other LEVONORGESTREL; ETHINYL ESTRADIOL Pharmaceutical Manufacturers / Labelers: