TEMODAR (Merck Sharp & Dohme Corp.)
Welcome to the PulseAid listing for the TEMODAR drug offered from Merck Sharp & Dohme Corp.. 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: | Merck Sharp & Dohme Corp. |
NON-PROPRIETARY NAME: | Temozolomide |
SUBSTANCE NAME: | TEMOZOLOMIDE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Alkylating Activity [MoA],Alkylating Drug [EPC] |
ROUTE: | INTRAVENOUS |
DOSAGE FORM: | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2009-02-27 |
END MARKETING DATE: | 0000-00-00 |
TEMODAR HUMAN PRESCRIPTION DRUG Details:
Item Description | TEMODAR from Merck Sharp & Dohme Corp. |
LABELER NAME: | Merck Sharp & Dohme Corp. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 2.5(mg/mL) |
START MARKETING DATE: | 2009-02-27 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0085-1381_41e18e8c-a81f-4ff1-a4a9-4434c709b059 |
PRODUCT NDC: | 0085-1381 |
APPLICATION NUMBER: | NDA022277 |
Other TEMOZOLOMIDE Pharmaceutical Manufacturers / Labelers: