Ifosfamide (APP Pharmaceuticals, LLC)
Welcome to the PulseAid listing for the Ifosfamide drug offered from APP Pharmaceuticals, LLC. This Alkylating Activity [MoA],Alkylating Drug [EPC] 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: | APP Pharmaceuticals, LLC |
NON-PROPRIETARY NAME: | IFOSFAMIDE |
SUBSTANCE NAME: | IFOSFAMIDE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Alkylating Activity [MoA],Alkylating Drug [EPC] |
ROUTE: | INTRAVENOUS |
DOSAGE FORM: | INJECTION, SOLUTION |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2009-09-30 |
END MARKETING DATE: | 0000-00-00 |
Ifosfamide HUMAN PRESCRIPTION DRUG Details:
Item Description | Ifosfamide from APP Pharmaceuticals, LLC |
LABELER NAME: | APP Pharmaceuticals, LLC |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 50(mg/mL) |
START MARKETING DATE: | 2009-09-30 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 63323-174_cb3778b6-f8a9-443d-8914-c5a25d22bd36 |
PRODUCT NDC: | 63323-174 |
APPLICATION NUMBER: | ANDA090181 |
Other IFOSFAMIDE Pharmaceutical Manufacturers / Labelers: