Bismatrol - 17856-1313-3 - (Bismuth Subsalicylate)

Alphabetical Index


Drug Information of Bismatrol

Product NDC: 17856-1313
Proprietary Name: Bismatrol
Non Proprietary Name: Bismuth Subsalicylate
Active Ingredient(s): 262    mg/15mL & nbsp;   Bismuth Subsalicylate
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Bismatrol

Product NDC: 17856-1313
Labeler Name: Atlantic Biologicals Corps
Product Type: HUMAN OTC DRUG
FDA Application Number: part335
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20080530

Package Information of Bismatrol

Package NDC: 17856-1313-3
Package Description: 30 mL in 1 CUP (17856-1313-3)

NDC Information of Bismatrol

NDC Code 17856-1313-3
Proprietary Name Bismatrol
Package Description 30 mL in 1 CUP (17856-1313-3)
Product NDC 17856-1313
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Bismuth Subsalicylate
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20080530
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Atlantic Biologicals Corps
Substance Name BISMUTH SUBSALICYLATE
Strength Number 262
Strength Unit mg/15mL
Pharmaceutical Classes

Complete Information of Bismatrol


General Information