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 DescriptionLevonorgestrel and Ethinyl Estradiol from Glenmark Pharmaceuticals Inc., USA
LABELER NAME: Glenmark Pharmaceuticals Inc., USA
DEA SCHEDULE:
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:

Manufacturer / LabelerProprietary Name
Actavis Pharma, Inc.Amethyst
Glenmark Pharmaceuticals Inc., USALevonorgestrel and Ethinyl Estradiol