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Bisacodyl Laxative - 50804-190-03 - (Bisacodyl)

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Drug Information of Bisacodyl Laxative

Product NDC: 50804-190
Proprietary Name: Bisacodyl Laxative
Non Proprietary Name: Bisacodyl
Active Ingredient(s): 5    mg/1 & nbsp;   Bisacodyl
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Bisacodyl Laxative

Product NDC: 50804-190
Labeler Name: Geiss, Destin & Dunn, Inc (Goodsense)
Product Type: HUMAN OTC DRUG
FDA Application Number: part334
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20100716

Package Information of Bisacodyl Laxative

Package NDC: 50804-190-03
Package Description: 1 BLISTER PACK in 1 CARTON (50804-190-03) > 25 TABLET, COATED in 1 BLISTER PACK

NDC Information of Bisacodyl Laxative

NDC Code 50804-190-03
Proprietary Name Bisacodyl Laxative
Package Description 1 BLISTER PACK in 1 CARTON (50804-190-03) > 25 TABLET, COATED in 1 BLISTER PACK
Product NDC 50804-190
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Bisacodyl
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20100716
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Geiss, Destin & Dunn, Inc (Goodsense)
Substance Name BISACODYL
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Bisacodyl Laxative


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