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Pamidronate Disodium - 55390-204-01 - (Pamidronate Disodium)

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Drug Information of Pamidronate Disodium

Product NDC: 55390-204
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: 55390-204
Labeler Name: Bedford Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021113
Marketing Category: NDA
Start Marketing Date: 20020312

Package Information of Pamidronate Disodium

Package NDC: 55390-204-01
Package Description: 1 VIAL in 1 BOX, UNIT-DOSE (55390-204-01) > 10 mL in 1 VIAL

NDC Information of Pamidronate Disodium

NDC Code 55390-204-01
Proprietary Name Pamidronate Disodium
Package Description 1 VIAL in 1 BOX, UNIT-DOSE (55390-204-01) > 10 mL in 1 VIAL
Product NDC 55390-204
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pamidronate Disodium
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20020312
Marketing Category Name NDA
Labeler Name Bedford Laboratories
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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