Norethindrone (Glenmark Pharmaceuticals Inc., USA)
Welcome to the PulseAid listing for the Norethindrone drug offered from Glenmark Pharmaceuticals Inc., USA. This 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 |
SUBSTANCE NAME: | NORETHINDRONE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Progesterone Congeners [Chemical/Ingredient],Progestin [EPC] |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2010-11-03 |
END MARKETING DATE: | 0000-00-00 |
Norethindrone HUMAN PRESCRIPTION DRUG Details:
Item Description | Norethindrone from Glenmark Pharmaceuticals Inc., USA |
LABELER NAME: | Glenmark Pharmaceuticals Inc., USA |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 0.35(mg/1) |
START MARKETING DATE: | 2010-11-03 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 68462-305_336e6f7b-ba28-4b88-9908-ae3d47be8ead |
PRODUCT NDC: | 68462-305 |
APPLICATION NUMBER: | ANDA091209 |
Other NORETHINDRONE Pharmaceutical Manufacturers / Labelers: