Home > National Drug Code (NDC) > Alendronate Sodium

Alendronate Sodium - 54868-5860-1 - (Alendronate Sodium)

Alphabetical Index


Drug Information of Alendronate Sodium

Product NDC: 54868-5860
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: 54868-5860
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075710
Marketing Category: ANDA
Start Marketing Date: 20080207

Package Information of Alendronate Sodium

Package NDC: 54868-5860-1
Package Description: 3 BOX in 1 CONTAINER (54868-5860-1) > 4 BLISTER PACK in 1 BOX > 1 TABLET in 1 BLISTER PACK

NDC Information of Alendronate Sodium

NDC Code 54868-5860-1
Proprietary Name Alendronate Sodium
Package Description 3 BOX in 1 CONTAINER (54868-5860-1) > 4 BLISTER PACK in 1 BOX > 1 TABLET in 1 BLISTER PACK
Product NDC 54868-5860
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Alendronate Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080207
Marketing Category Name ANDA
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 Alendronate Sodium


General Information