AMIFOSTINE (Sun Pharmaceutical Industries Limited)
Welcome to the PulseAid listing for the AMIFOSTINE drug offered from Sun Pharmaceutical Industries Limited. 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: | Sun Pharmaceutical Industries Limited |
| NON-PROPRIETARY NAME: | AMIFOSTINE |
| SUBSTANCE NAME: | AMIFOSTINE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | |
| ROUTE: | INTRAVENOUS |
| DOSAGE FORM: | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2008-03-14 |
| END MARKETING DATE: | 0000-00-00 |
AMIFOSTINE HUMAN PRESCRIPTION DRUG Details:
| Item Description | AMIFOSTINE from Sun Pharmaceutical Industries Limited |
| LABELER NAME: | Sun Pharmaceutical Industries Limited |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 50(mg/mL) |
| START MARKETING DATE: | 2008-03-14 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 62756-581_2a527ed0-3af2-41eb-9e8f-5b4783b37259 |
| PRODUCT NDC: | 62756-581 |
| APPLICATION NUMBER: | ANDA077126 |
Other AMIFOSTINE Pharmaceutical Manufacturers / Labelers:
