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Alendronate Sodium - 60505-2596-8 - (Alendronate Sodium)

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Drug Information of Alendronate Sodium

Product NDC: 60505-2596
Proprietary Name: Alendronate Sodium
Non Proprietary Name: Alendronate Sodium
Active Ingredient(s): 70    mg/1 & nbsp;   Alendronate Sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Alendronate Sodium

Product NDC: 60505-2596
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077982
Marketing Category: ANDA
Start Marketing Date: 20080804

Package Information of Alendronate Sodium

Package NDC: 60505-2596-8
Package Description: 1000 TABLET in 1 BOTTLE (60505-2596-8)

NDC Information of Alendronate Sodium

NDC Code 60505-2596-8
Proprietary Name Alendronate Sodium
Package Description 1000 TABLET in 1 BOTTLE (60505-2596-8)
Product NDC 60505-2596
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Alendronate Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080804
Marketing Category Name ANDA
Labeler Name Apotex Corp.
Substance Name ALENDRONATE SODIUM
Strength Number 70
Strength Unit mg/1
Pharmaceutical Classes Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient]

Complete Information of Alendronate Sodium


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