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Zoledronic Acid - 55111-688-52 - (Zoledronic Acid)

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Drug Information of Zoledronic Acid

Product NDC: 55111-688
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: 55111-688
Labeler Name: Dr.Reddy's Laboratories Ltd
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091363
Marketing Category: ANDA
Start Marketing Date: 20130403

Package Information of Zoledronic Acid

Package NDC: 55111-688-52
Package Description: 100 mL in 1 BOTTLE, GLASS (55111-688-52)

NDC Information of Zoledronic Acid

NDC Code 55111-688-52
Proprietary Name Zoledronic Acid
Package Description 100 mL in 1 BOTTLE, GLASS (55111-688-52)
Product NDC 55111-688
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Zoledronic Acid
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20130403
Marketing Category Name ANDA
Labeler Name Dr.Reddy's Laboratories Ltd
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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