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Alendronate Sodium - 51079-942-05 - (Alendronate Sodium)

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Drug Information of Alendronate Sodium

Product NDC: 51079-942
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: 51079-942
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076584
Marketing Category: ANDA
Start Marketing Date: 20111006

Package Information of Alendronate Sodium

Package NDC: 51079-942-05
Package Description: 20 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-942-05) > 1 TABLET in 1 BLISTER PACK (51079-942-01)

NDC Information of Alendronate Sodium

NDC Code 51079-942-05
Proprietary Name Alendronate Sodium
Package Description 20 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-942-05) > 1 TABLET in 1 BLISTER PACK (51079-942-01)
Product NDC 51079-942
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Alendronate Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111006
Marketing Category Name ANDA
Labeler Name UDL Laboratories, 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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