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Pamidronate Disodium - 61703-356-18 - (PAMIDRONATE DISODIUM)

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Drug Information of Pamidronate Disodium

Product NDC: 61703-356
Proprietary Name: Pamidronate Disodium
Non Proprietary Name: PAMIDRONATE DISODIUM
Active Ingredient(s): 9    mg/mL & nbsp;   PAMIDRONATE DISODIUM
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Pamidronate Disodium

Product NDC: 61703-356
Labeler Name: Hospira Worldwide, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075841
Marketing Category: ANDA
Start Marketing Date: 20110623

Package Information of Pamidronate Disodium

Package NDC: 61703-356-18
Package Description: 1 VIAL in 1 CARTON (61703-356-18) > 10 mL in 1 VIAL

NDC Information of Pamidronate Disodium

NDC Code 61703-356-18
Proprietary Name Pamidronate Disodium
Package Description 1 VIAL in 1 CARTON (61703-356-18) > 10 mL in 1 VIAL
Product NDC 61703-356
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PAMIDRONATE DISODIUM
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20110623
Marketing Category Name ANDA
Labeler Name Hospira Worldwide, Inc.
Substance Name PAMIDRONATE DISODIUM
Strength Number 9
Strength Unit mg/mL
Pharmaceutical Classes Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient]

Complete Information of Pamidronate Disodium


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