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FOSAMAX PLUS D - 0006-0710-44 - (ALENDRONATE SODIUM and CHOLECALCIFEROL)

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Drug Information of FOSAMAX PLUS D

Product NDC: 0006-0710
Proprietary Name: FOSAMAX PLUS D
Non Proprietary Name: ALENDRONATE SODIUM and CHOLECALCIFEROL
Active Ingredient(s): 70; 2800    mg/1; [iU]/1 & nbsp;   ALENDRONATE SODIUM and CHOLECALCIFEROL
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of FOSAMAX PLUS D

Product NDC: 0006-0710
Labeler Name: Merck Sharp & Dohme Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021762
Marketing Category: NDA
Start Marketing Date: 20050407

Package Information of FOSAMAX PLUS D

Package NDC: 0006-0710-44
Package Description: 4 TABLET in 1 BLISTER PACK (0006-0710-44)

NDC Information of FOSAMAX PLUS D

NDC Code 0006-0710-44
Proprietary Name FOSAMAX PLUS D
Package Description 4 TABLET in 1 BLISTER PACK (0006-0710-44)
Product NDC 0006-0710
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ALENDRONATE SODIUM and CHOLECALCIFEROL
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050407
Marketing Category Name NDA
Labeler Name Merck Sharp & Dohme Corp.
Substance Name ALENDRONATE SODIUM; CHOLECALCIFEROL
Strength Number 70; 2800
Strength Unit mg/1; [iU]/1
Pharmaceutical Classes Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient],Vitamin D [Chemical/Ingredient],Vitamin D [EPC]

Complete Information of FOSAMAX PLUS D


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