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 |