Zoledronic Acid (Breckenridge Pharmaceutical, Inc)
Welcome to the PulseAid listing for the Zoledronic Acid drug offered from Breckenridge Pharmaceutical, Inc. 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: | Breckenridge Pharmaceutical, Inc |
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 |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2017-09-15 |
END MARKETING DATE: | 0000-00-00 |
Zoledronic Acid HUMAN PRESCRIPTION DRUG Details:
Item Description | Zoledronic Acid from Breckenridge Pharmaceutical, Inc |
LABELER NAME: | Breckenridge Pharmaceutical, Inc |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 5(mg/100mL) |
START MARKETING DATE: | 2017-09-15 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 51991-064_528eda32-9c82-42e0-883b-13ef563c7d91 |
PRODUCT NDC: | 51991-064 |
APPLICATION NUMBER: | ANDA202163 |
Other ZOLEDRONIC ACID Pharmaceutical Manufacturers / Labelers: