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Medique Diotame - 47682-220-33 - (BISMUTH SUBSALICYLATE)

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Drug Information of Medique Diotame

Product NDC: 47682-220
Proprietary Name: Medique Diotame
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 Medique Diotame

Product NDC: 47682-220
Labeler Name: Unifirst First Aid Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part335
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20081230

Package Information of Medique Diotame

Package NDC: 47682-220-33
Package Description: 50 PACKET in 1 BOX, UNIT-DOSE (47682-220-33) > 2 TABLET, CHEWABLE in 1 PACKET (47682-220-99)

NDC Information of Medique Diotame

NDC Code 47682-220-33
Proprietary Name Medique Diotame
Package Description 50 PACKET in 1 BOX, UNIT-DOSE (47682-220-33) > 2 TABLET, CHEWABLE in 1 PACKET (47682-220-99)
Product NDC 47682-220
Product Type Name HUMAN OTC DRUG
Non Proprietary Name BISMUTH SUBSALICYLATE
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20081230
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Unifirst First Aid Corporation
Substance Name BISMUTH SUBSALICYLATE
Strength Number 262
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Medique Diotame


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