Zometa (Novartis Pharmaceuticals Corporation)
Welcome to the PulseAid listing for the Zometa drug offered from Novartis Pharmaceuticals Corporation. This Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient] 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: | Novartis Pharmaceuticals Corporation |
| NON-PROPRIETARY NAME: | zoledronic acid |
| SUBSTANCE NAME: | ZOLEDRONIC ACID |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient] |
| ROUTE: | INTRAVENOUS |
| DOSAGE FORM: | INJECTION, SOLUTION, CONCENTRATE |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 2001-08-20 |
| END MARKETING DATE: | 0000-00-00 |
Zometa HUMAN PRESCRIPTION DRUG Details:
| Item Description | Zometa from Novartis Pharmaceuticals Corporation |
| LABELER NAME: | Novartis Pharmaceuticals Corporation |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 4(mg/5mL) |
| START MARKETING DATE: | 2001-08-20 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0078-0387_993aa2f3-5d6f-4816-9315-5904cbc16757 |
| PRODUCT NDC: | 0078-0387 |
| APPLICATION NUMBER: | NDA021223 |
Other ZOLEDRONIC ACID Pharmaceutical Manufacturers / Labelers:
