Norethindrone Acetate and Ethinyl Estradiol and Ferrous Fumarate (Actavis Pharma, Inc.)
Welcome to the PulseAid listing for the Norethindrone Acetate and Ethinyl Estradiol and Ferrous Fumarate drug offered from Actavis Pharma, Inc.. This 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: | Actavis Pharma, Inc. |
NON-PROPRIETARY NAME: | Norethindrone Acetate and Ethinyl Estradiol and Ferrous Fumarate |
SUBSTANCE NAME: | |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | |
ROUTE: | |
DOSAGE FORM: | KIT |
MARKETING CATEGORY NAME: | NDA AUTHORIZED GENERIC |
START MARKETING DATE: | 2017-03-16 |
END MARKETING DATE: | 0000-00-00 |
Norethindrone Acetate and Ethinyl Estradiol and Ferrous Fumarate HUMAN PRESCRIPTION DRUG Details:
Item Description | Norethindrone Acetate and Ethinyl Estradiol and Ferrous Fumarate from Actavis Pharma, Inc. |
LABELER NAME: | Actavis Pharma, Inc. |
DEA SCHEDULE: | |
ACTIVE STRENGTH: | () |
START MARKETING DATE: | 2017-03-16 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 52544-058_068d36bf-2c22-4298-a74e-4993469a88ff |
PRODUCT NDC: | 52544-058 |
APPLICATION NUMBER: | NDA203667 |