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Alendronate Sodium - 0093-5172-20 - (Alendronate Sodium)

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Drug Information of Alendronate Sodium

Product NDC: 0093-5172
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: 0093-5172
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075710
Marketing Category: ANDA
Start Marketing Date: 20080206

Package Information of Alendronate Sodium

Package NDC: 0093-5172-20
Package Description: 20 BLISTER PACK in 1 PACKAGE (0093-5172-20) > 1 TABLET in 1 BLISTER PACK (0093-5172-19)

NDC Information of Alendronate Sodium

NDC Code 0093-5172-20
Proprietary Name Alendronate Sodium
Package Description 20 BLISTER PACK in 1 PACKAGE (0093-5172-20) > 1 TABLET in 1 BLISTER PACK (0093-5172-19)
Product NDC 0093-5172
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Alendronate Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080206
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA 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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