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Bismuth Subsalicylate - 62211-046-99 - (Bismuth Subsalicylate)

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Drug Information of Bismuth Subsalicylate

Product NDC: 62211-046
Proprietary Name: Bismuth Subsalicylate
Non Proprietary Name: Bismuth Subsalicylate
Active Ingredient(s): 262    mg/1 & nbsp;   Bismuth Subsalicylate
Administration Route(s): ORAL
Dosage Form(s): TABLET, CHEWABLE
Coding System: National Drug Codes(NDC)

Labeler Information of Bismuth Subsalicylate

Product NDC: 62211-046
Labeler Name: A&Z Pharmaceutical, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part335
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20030310

Package Information of Bismuth Subsalicylate

Package NDC: 62211-046-99
Package Description: 15000 TABLET, CHEWABLE in 1 CARTON (62211-046-99)

NDC Information of Bismuth Subsalicylate

NDC Code 62211-046-99
Proprietary Name Bismuth Subsalicylate
Package Description 15000 TABLET, CHEWABLE in 1 CARTON (62211-046-99)
Product NDC 62211-046
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Bismuth Subsalicylate
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20030310
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name A&Z Pharmaceutical, Inc.
Substance Name BISMUTH SUBSALICYLATE
Strength Number 262
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Bismuth Subsalicylate


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