Temozolomide (Kremers Urban Pharmaceuticals Inc.)
Welcome to the PulseAid listing for the Temozolomide drug offered from Kremers Urban Pharmaceuticals 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: | Kremers Urban Pharmaceuticals 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: | ANDA |
| START MARKETING DATE: | 2016-02-10 |
| END MARKETING DATE: | 0000-00-00 |
Temozolomide HUMAN PRESCRIPTION DRUG Details:
| Item Description | Temozolomide from Kremers Urban Pharmaceuticals Inc. |
| LABELER NAME: | Kremers Urban Pharmaceuticals Inc. |
| DEA SCHEDULE: |
|
| ACTIVE STRENGTH: | 5(mg/1) |
| START MARKETING DATE: | 2016-02-10 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 62175-240_665c8d06-381d-4217-9cdb-8d837733e918 |
| PRODUCT NDC: | 62175-240 |
| APPLICATION NUMBER: | ANDA203898 |
Other TEMOZOLOMIDE Pharmaceutical Manufacturers / Labelers:
