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Pamidronate Disodium - 0069-0107-01 - (Pamidronate Disodium)

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Drug Information of Pamidronate Disodium

Product NDC: 0069-0107
Proprietary Name: Pamidronate Disodium
Non Proprietary Name: Pamidronate Disodium
Active Ingredient(s): 3    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: 0069-0107
Labeler Name: Pfizer Laboratories Div Pfizer Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078520
Marketing Category: ANDA
Start Marketing Date: 20110510

Package Information of Pamidronate Disodium

Package NDC: 0069-0107-01
Package Description: 10 mL in 1 VIAL (0069-0107-01)

NDC Information of Pamidronate Disodium

NDC Code 0069-0107-01
Proprietary Name Pamidronate Disodium
Package Description 10 mL in 1 VIAL (0069-0107-01)
Product NDC 0069-0107
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pamidronate Disodium
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20110510
Marketing Category Name ANDA
Labeler Name Pfizer Laboratories Div Pfizer Inc
Substance Name PAMIDRONATE DISODIUM
Strength Number 3
Strength Unit mg/mL
Pharmaceutical Classes Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient]

Complete Information of Pamidronate Disodium


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