Fludrocortisone Acetate (Teva Pharmaceuticals USA, Inc.)
Welcome to the PulseAid listing for the Fludrocortisone Acetate 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: | Fludrocortisone Acetate |
SUBSTANCE NAME: | FLUDROCORTISONE ACETATE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2003-02-14 |
END MARKETING DATE: | 0000-00-00 |
Fludrocortisone Acetate HUMAN PRESCRIPTION DRUG Details:
Item Description | Fludrocortisone Acetate from Teva Pharmaceuticals USA, Inc. |
LABELER NAME: | Teva Pharmaceuticals USA, Inc. |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 0.1(mg/1) |
START MARKETING DATE: | 2003-02-14 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0555-0997_b61dc31b-5cf1-4fd7-8a8d-4fd6c33a383c |
PRODUCT NDC: | 0555-0997 |
APPLICATION NUMBER: | ANDA040425 |
Other FLUDROCORTISONE ACETATE Pharmaceutical Manufacturers / Labelers: