Pamidronate Disodium (APP Pharmaceuticals, LLC)
Welcome to the PulseAid listing for the Pamidronate Disodium drug offered from APP Pharmaceuticals, 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: | APP Pharmaceuticals, LLC |
NON-PROPRIETARY NAME: | PAMIDRONATE DISODIUM |
SUBSTANCE NAME: | PAMIDRONATE DISODIUM |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient] |
ROUTE: | INTRAVENOUS |
DOSAGE FORM: | INJECTION, SOLUTION |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2002-05-19 |
END MARKETING DATE: | 0000-00-00 |
Pamidronate Disodium HUMAN PRESCRIPTION DRUG Details:
Item Description | Pamidronate Disodium from APP Pharmaceuticals, LLC |
LABELER NAME: | APP Pharmaceuticals, LLC |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 3(mg/mL) |
START MARKETING DATE: | 2002-05-19 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 63323-734_80ed4c20-1e43-4fe2-bfd9-64652ba75471 |
PRODUCT NDC: | 63323-734 |
APPLICATION NUMBER: | ANDA076207 |
Other PAMIDRONATE DISODIUM Pharmaceutical Manufacturers / Labelers: