HYDROXYUREA (Teva Pharmaceuticals USA Inc)
Welcome to the PulseAid listing for the HYDROXYUREA drug offered from Teva Pharmaceuticals USA Inc. This Antimetabolite [EPC],Urea [Chemical/Ingredient] 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: | Hydroxyurea |
| SUBSTANCE NAME: | HYDROXYUREA |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Antimetabolite [EPC],Urea [Chemical/Ingredient] |
| ROUTE: | ORAL |
| DOSAGE FORM: | CAPSULE |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 1998-10-19 |
| END MARKETING DATE: | 0000-00-00 |
HYDROXYUREA HUMAN PRESCRIPTION DRUG Details:
| Item Description | HYDROXYUREA from Teva Pharmaceuticals USA Inc |
| LABELER NAME: | Teva Pharmaceuticals USA Inc |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 500(mg/1) |
| START MARKETING DATE: | 1998-10-19 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0555-0882_3b9c9ccf-3d3b-4208-89b9-7bdfc6e6b577 |
| PRODUCT NDC: | 0555-0882 |
| APPLICATION NUMBER: | ANDA075143 |
Other HYDROXYUREA Pharmaceutical Manufacturers / Labelers:
