Dacarbazine (Teva Parenteral Medicines, Inc.)
Welcome to the PulseAid listing for the Dacarbazine drug offered from Teva Parenteral Medicines, Inc.. 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: | Teva Parenteral Medicines, Inc. |
NON-PROPRIETARY NAME: | Dacarbazine |
SUBSTANCE NAME: | DACARBAZINE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Alkylating Activity [MoA],Alkylating Drug [EPC] |
ROUTE: | INTRAVENOUS |
DOSAGE FORM: | INJECTION, POWDER, FOR SOLUTION |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 1998-08-27 |
END MARKETING DATE: | 0000-00-00 |
Dacarbazine HUMAN PRESCRIPTION DRUG Details:
Item Description | Dacarbazine from Teva Parenteral Medicines, Inc. |
LABELER NAME: | Teva Parenteral Medicines, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 200(mg/20mL) |
START MARKETING DATE: | 1998-08-27 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0703-5075_308fc8a0-221e-4c2f-8c88-b20ae3846f89 |
PRODUCT NDC: | 0703-5075 |
APPLICATION NUMBER: | ANDA075259 |
Other DACARBAZINE Pharmaceutical Manufacturers / Labelers: