Temozolomide (Sandoz Inc.)
Welcome to the PulseAid listing for the Temozolomide drug offered from Sandoz 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: | Sandoz Inc. |
| NON-PROPRIETARY NAME: | Temozolomide |
| SUBSTANCE NAME: | TEMOZOLOMIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Alkylating Activity [MoA],Alkylating Drug [EPC] |
| ROUTE: | ORAL |
| DOSAGE FORM: | CAPSULE |
| MARKETING CATEGORY NAME: | NDA AUTHORIZED GENERIC |
| START MARKETING DATE: | 2013-08-12 |
| END MARKETING DATE: | 0000-00-00 |
Temozolomide HUMAN PRESCRIPTION DRUG Details:
| Item Description | Temozolomide from Sandoz Inc. |
| LABELER NAME: | Sandoz Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 5(mg/1) |
| START MARKETING DATE: | 2013-08-12 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0781-2691_a750842d-b4f8-4569-9b94-e0520a4d21af |
| PRODUCT NDC: | 0781-2691 |
| APPLICATION NUMBER: | NDA021029 |
Other TEMOZOLOMIDE Pharmaceutical Manufacturers / Labelers:
