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Alendronate Sodium - 16252-599-00 - (alendronate sodium)

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Drug Information of Alendronate Sodium

Product NDC: 16252-599
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: 16252-599
Labeler Name: Cobalt Laboratories Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076984
Marketing Category: ANDA
Start Marketing Date: 20091023

Package Information of Alendronate Sodium

Package NDC: 16252-599-00
Package Description: 50000 TABLET in 1 PAIL (16252-599-00)

NDC Information of Alendronate Sodium

NDC Code 16252-599-00
Proprietary Name Alendronate Sodium
Package Description 50000 TABLET in 1 PAIL (16252-599-00)
Product NDC 16252-599
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name alendronate sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091023
Marketing Category Name ANDA
Labeler Name Cobalt Laboratories 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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