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Alendronate Sodium - 41616-638-68 - (Alendronate Sodium)

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Drug Information of Alendronate Sodium

Product NDC: 41616-638
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: 41616-638
Labeler Name: SUN PHARMA GLOBAL INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090022
Marketing Category: ANDA
Start Marketing Date: 20080910

Package Information of Alendronate Sodium

Package NDC: 41616-638-68
Package Description: 1 BLISTER PACK in 1 CARTON (41616-638-68) > 4 TABLET in 1 BLISTER PACK

NDC Information of Alendronate Sodium

NDC Code 41616-638-68
Proprietary Name Alendronate Sodium
Package Description 1 BLISTER PACK in 1 CARTON (41616-638-68) > 4 TABLET in 1 BLISTER PACK
Product NDC 41616-638
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Alendronate Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080910
Marketing Category Name ANDA
Labeler Name SUN PHARMA GLOBAL INC.
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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