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Pamidronate Disodium - 0703-4075-51 - (Pamidronate Disodium)

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Drug Information of Pamidronate Disodium

Product NDC: 0703-4075
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: 0703-4075
Labeler Name: Teva Parenteral Medicines, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076153
Marketing Category: ANDA
Start Marketing Date: 20020401

Package Information of Pamidronate Disodium

Package NDC: 0703-4075-51
Package Description: 1 VIAL, SINGLE-DOSE in 1 CARTON (0703-4075-51) > 10 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Pamidronate Disodium

NDC Code 0703-4075-51
Proprietary Name Pamidronate Disodium
Package Description 1 VIAL, SINGLE-DOSE in 1 CARTON (0703-4075-51) > 10 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0703-4075
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pamidronate Disodium
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20020401
Marketing Category Name ANDA
Labeler Name Teva Parenteral Medicines, 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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