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Alendronate Sodium - 65862-329-10 - (Alendronate Sodium)

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Drug Information of Alendronate Sodium

Product NDC: 65862-329
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: 65862-329
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090124
Marketing Category: ANDA
Start Marketing Date: 20080804

Package Information of Alendronate Sodium

Package NDC: 65862-329-10
Package Description: 10 BLISTER PACK in 1 CARTON (65862-329-10) > 10 TABLET in 1 BLISTER PACK

NDC Information of Alendronate Sodium

NDC Code 65862-329-10
Proprietary Name Alendronate Sodium
Package Description 10 BLISTER PACK in 1 CARTON (65862-329-10) > 10 TABLET in 1 BLISTER PACK
Product NDC 65862-329
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 Aurobindo Pharma Limited
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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