Jolessa (Teva Pharmaceuticals USA, Inc.)
Welcome to the PulseAid listing for the Jolessa 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: | Levonorgestrel / Ethinyl Estradiol |
SUBSTANCE NAME: | |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | |
ROUTE: | |
DOSAGE FORM: | KIT |
MARKETING CATEGORY NAME: | NDA AUTHORIZED GENERIC |
START MARKETING DATE: | 2003-10-13 |
END MARKETING DATE: | 0000-00-00 |
Jolessa HUMAN PRESCRIPTION DRUG Details:
Item Description | Jolessa from Teva Pharmaceuticals USA, Inc. |
LABELER NAME: | Teva Pharmaceuticals USA, Inc. |
DEA SCHEDULE: | |
ACTIVE STRENGTH: | () |
START MARKETING DATE: | 2003-10-13 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0555-9123_f51e16dc-1618-45f2-964b-1e0856adc2df |
PRODUCT NDC: | 0555-9123 |
APPLICATION NUMBER: | NDA021544 |