Fosamax - 54868-4463-0 - (alendronate sodium)

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Drug Information of Fosamax

Product NDC: 54868-4463
Proprietary Name: Fosamax
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 Fosamax

Product NDC: 54868-4463
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020560
Marketing Category: NDA
Start Marketing Date: 20010205

Package Information of Fosamax

Package NDC: 54868-4463-0
Package Description: 4 TABLET in 1 BOTTLE (54868-4463-0)

NDC Information of Fosamax

NDC Code 54868-4463-0
Proprietary Name Fosamax
Package Description 4 TABLET in 1 BOTTLE (54868-4463-0)
Product NDC 54868-4463
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name alendronate sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20010205
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name ALENDRONATE SODIUM
Strength Number 35
Strength Unit mg/1
Pharmaceutical Classes Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient]

Complete Information of Fosamax


General Information