Pamidronate Disodium (Hospira, Inc.)


Welcome to the PulseAid listing for the Pamidronate Disodium drug offered from Hospira, 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: Hospira, Inc.
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: 2005-10-01
END MARKETING DATE: 0000-00-00


Pamidronate Disodium HUMAN PRESCRIPTION DRUG Details:

Item DescriptionPamidronate Disodium from Hospira, Inc.
LABELER NAME: Hospira, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 3(mg/mL)
START MARKETING DATE: 2005-10-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 61703-324_32de72be-4532-4c8b-a9bf-7546414077eb
PRODUCT NDC: 61703-324
APPLICATION NUMBER: ANDA075841

Other PAMIDRONATE DISODIUM Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
American Regent, Inc.Pamidronate Disodium
APP Pharmaceuticals, LLCPamidronate Disodium
Areva Pharmaceuticals Inc.Pamidronate Disodium
Hospira, Inc.Pamidronate Disodium
Mylan Institutional LLCPamidronate Disodium
Pfizer Laboratories Div Pfizer IncPamidronate Disodium
Teva Parenteral Medicines, Inc.Pamidronate Disodium