Activella (Gemini Laboratories, LLC)
Welcome to the PulseAid listing for the Activella drug offered from Gemini Laboratories, LLC. This Estradiol Congeners [Chemical/Ingredient],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: | Gemini Laboratories, LLC |
NON-PROPRIETARY NAME: | estradiol and norethindrone acetate |
SUBSTANCE NAME: | ESTRADIOL; NORETHINDRONE ACETATE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Estradiol Congeners [Chemical/Ingredient],Estrogen [EPC],Estrogen Receptor Agonists [MoA],Progesterone Congeners [Chemical/Ingredient],Progestin [EPC] |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET, FILM COATED |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2016-05-12 |
END MARKETING DATE: | 0000-00-00 |
Activella HUMAN PRESCRIPTION DRUG Details:
Item Description | Activella from Gemini Laboratories, LLC |
LABELER NAME: | Gemini Laboratories, LLC |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | .5; .1(mg/1; mg/1) |
START MARKETING DATE: | 2016-05-12 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 60846-201_57e6f8e3-d587-71bb-e053-2991aa0aabe6 |
PRODUCT NDC: | 60846-201 |
APPLICATION NUMBER: | NDA020907 |
Other ESTRADIOL; NORETHINDRONE ACETATE Pharmaceutical Manufacturers / Labelers: