DROXIA (E.R. Squibb & Sons, L.L.C.)
Welcome to the PulseAid listing for the DROXIA drug offered from E.R. Squibb & Sons, L.L.C.. 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: | E.R. Squibb & Sons, L.L.C. |
| 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: | NDA |
| START MARKETING DATE: | 2009-06-01 |
| END MARKETING DATE: | 0000-00-00 |
DROXIA HUMAN PRESCRIPTION DRUG Details:
| Item Description | DROXIA from E.R. Squibb & Sons, L.L.C. |
| LABELER NAME: | E.R. Squibb & Sons, L.L.C. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 200(mg/1) |
| START MARKETING DATE: | 2009-06-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0003-6335_a8bc29c3-232a-445e-831d-f167031da663 |
| PRODUCT NDC: | 0003-6335 |
| APPLICATION NUMBER: | NDA016295 |
Other HYDROXYUREA Pharmaceutical Manufacturers / Labelers:
