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ALENDRONATE SODIUM - 24658-162-73 - (ALENDRONATE SODIUM)

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Drug Information of ALENDRONATE SODIUM

Product NDC: 24658-162
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: 24658-162
Labeler Name: Blu Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090258
Marketing Category: ANDA
Start Marketing Date: 20130205

Package Information of ALENDRONATE SODIUM

Package NDC: 24658-162-73
Package Description: 3 BLISTER PACK in 1 CARTON (24658-162-73) > 4 TABLET in 1 BLISTER PACK (24658-162-71)

NDC Information of ALENDRONATE SODIUM

NDC Code 24658-162-73
Proprietary Name ALENDRONATE SODIUM
Package Description 3 BLISTER PACK in 1 CARTON (24658-162-73) > 4 TABLET in 1 BLISTER PACK (24658-162-71)
Product NDC 24658-162
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ALENDRONATE SODIUM
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130205
Marketing Category Name ANDA
Labeler Name Blu Pharmaceuticals, LLC
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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