Femring (Warner Chilcott (US), LLC)
Welcome to the PulseAid listing for the Femring drug offered from Warner Chilcott (US), LLC. This Estradiol Congeners [Chemical/Ingredient],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: | Warner Chilcott (US), LLC |
NON-PROPRIETARY NAME: | estradiol acetate |
SUBSTANCE NAME: | ESTRADIOL ACETATE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Estradiol Congeners [Chemical/Ingredient],Estrogen [EPC],Estrogen Receptor Agonists [MoA] |
ROUTE: | VAGINAL |
DOSAGE FORM: | RING |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2003-07-01 |
END MARKETING DATE: | 0000-00-00 |
Femring HUMAN PRESCRIPTION DRUG Details:
Item Description | Femring from Warner Chilcott (US), LLC |
LABELER NAME: | Warner Chilcott (US), LLC |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 0.05(mg/d) |
START MARKETING DATE: | 2003-07-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0430-6201_4c5203e4-6c37-4dbc-a4a1-caa118b72c95 |
PRODUCT NDC: | 0430-6201 |
APPLICATION NUMBER: | NDA021367 |
Other ESTRADIOL ACETATE Pharmaceutical Manufacturers / Labelers: