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Alendronate Sodium - 59746-242-02 - (Alendronate Sodium)

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Drug Information of Alendronate Sodium

Product NDC: 59746-242
Proprietary Name: Alendronate Sodium
Non Proprietary Name: Alendronate Sodium
Active Ingredient(s): 35    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: 59746-242
Labeler Name: Jubilant Cadista Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090557
Marketing Category: ANDA
Start Marketing Date: 20110701

Package Information of Alendronate Sodium

Package NDC: 59746-242-02
Package Description: 4 TABLET in 1 BLISTER PACK (59746-242-02)

NDC Information of Alendronate Sodium

NDC Code 59746-242-02
Proprietary Name Alendronate Sodium
Package Description 4 TABLET in 1 BLISTER PACK (59746-242-02)
Product NDC 59746-242
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Alendronate Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110701
Marketing Category Name ANDA
Labeler Name Jubilant Cadista Pharmaceuticals Inc.
Substance Name ALENDRONATE SODIUM
Strength Number 35
Strength Unit mg/1
Pharmaceutical Classes Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient]

Complete Information of Alendronate Sodium


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