Zoledronic Acid (Amneal-Agila, LLC)
Welcome to the PulseAid listing for the Zoledronic Acid drug offered from Amneal-Agila, LLC. 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: | Amneal-Agila, LLC |
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: | ANDA |
START MARKETING DATE: | 2012-04-23 |
END MARKETING DATE: | 0000-00-00 |
Zoledronic Acid HUMAN PRESCRIPTION DRUG Details:
Item Description | Zoledronic Acid from Amneal-Agila, LLC |
LABELER NAME: | Amneal-Agila, LLC |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 4(mg/5mL) |
START MARKETING DATE: | 2012-04-23 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 53150-871_d4595229-52b1-4ddb-8fcf-d9422406ca43 |
PRODUCT NDC: | 53150-871 |
APPLICATION NUMBER: | ANDA202650 |
Other ZOLEDRONIC ACID Pharmaceutical Manufacturers / Labelers: