OCELLA (TEVA PHARMACEUTICALS USA, INC.)
Welcome to the PulseAid listing for the OCELLA drug offered from TEVA PHARMACEUTICALS USA, 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: | TEVA PHARMACEUTICALS USA, INC. |
NON-PROPRIETARY NAME: | drospirenone and ethinyl estradiol |
SUBSTANCE NAME: | |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | |
ROUTE: | |
DOSAGE FORM: | KIT |
MARKETING CATEGORY NAME: | NDA AUTHORIZED GENERIC |
START MARKETING DATE: | 2001-06-11 |
END MARKETING DATE: | 0000-00-00 |
OCELLA HUMAN PRESCRIPTION DRUG Details:
Item Description | OCELLA from TEVA PHARMACEUTICALS USA, INC. |
LABELER NAME: | TEVA PHARMACEUTICALS USA, INC. |
DEA SCHEDULE: | |
ACTIVE STRENGTH: | () |
START MARKETING DATE: | 2001-06-11 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0555-9131_6daee173-c467-4f50-8cdb-ffd88500e543 |
PRODUCT NDC: | 0555-9131 |
APPLICATION NUMBER: | NDA021098 |