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Zoledronic Acid - 55648-186-01 - (Zoledronic Acid)

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Drug Information of Zoledronic Acid

Product NDC: 55648-186
Proprietary Name: Zoledronic Acid
Non Proprietary Name: Zoledronic Acid
Active Ingredient(s): 4    mg/5mL & nbsp;   Zoledronic Acid
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Zoledronic Acid

Product NDC: 55648-186
Labeler Name: Wockhardt Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA203069
Marketing Category: ANDA
Start Marketing Date: 20130302

Package Information of Zoledronic Acid

Package NDC: 55648-186-01
Package Description: 1 VIAL in 1 CARTON (55648-186-01) > 5 mL in 1 VIAL

NDC Information of Zoledronic Acid

NDC Code 55648-186-01
Proprietary Name Zoledronic Acid
Package Description 1 VIAL in 1 CARTON (55648-186-01) > 5 mL in 1 VIAL
Product NDC 55648-186
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Zoledronic Acid
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20130302
Marketing Category Name ANDA
Labeler Name Wockhardt Limited
Substance Name ZOLEDRONIC ACID
Strength Number 4
Strength Unit mg/5mL
Pharmaceutical Classes Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient]

Complete Information of Zoledronic Acid


General Information