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Zoledronic acid - 23155-186-31 - (Zoledronic acid)

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Drug Information of Zoledronic acid

Product NDC: 23155-186
Proprietary Name: Zoledronic acid
Non Proprietary Name: Zoledronic acid
Active Ingredient(s): 5    mg/100mL & nbsp;   Zoledronic acid
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Zoledronic acid

Product NDC: 23155-186
Labeler Name: Heritage Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201801
Marketing Category: ANDA
Start Marketing Date: 20121220

Package Information of Zoledronic acid

Package NDC: 23155-186-31
Package Description: 1 VIAL, GLASS in 1 CARTON (23155-186-31) > 100 mL in 1 VIAL, GLASS

NDC Information of Zoledronic acid

NDC Code 23155-186-31
Proprietary Name Zoledronic acid
Package Description 1 VIAL, GLASS in 1 CARTON (23155-186-31) > 100 mL in 1 VIAL, GLASS
Product NDC 23155-186
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Zoledronic acid
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20121220
Marketing Category Name ANDA
Labeler Name Heritage Pharmaceuticals Inc.
Substance Name ZOLEDRONIC ACID
Strength Number 5
Strength Unit mg/100mL
Pharmaceutical Classes Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient]

Complete Information of Zoledronic acid


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