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womens laxative - 50804-120-30 - (Bisacodyl)

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Drug Information of womens laxative

Product NDC: 50804-120
Proprietary Name: womens laxative
Non Proprietary Name: Bisacodyl
Active Ingredient(s): 5    mg/1 & nbsp;   Bisacodyl
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of womens laxative

Product NDC: 50804-120
Labeler Name: Good Sense (Geiss, Destin & Dunn, Inc.)
Product Type: HUMAN OTC DRUG
FDA Application Number: part334
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20130416

Package Information of womens laxative

Package NDC: 50804-120-30
Package Description: 2 BLISTER PACK in 1 CARTON (50804-120-30) > 15 TABLET in 1 BLISTER PACK

NDC Information of womens laxative

NDC Code 50804-120-30
Proprietary Name womens laxative
Package Description 2 BLISTER PACK in 1 CARTON (50804-120-30) > 15 TABLET in 1 BLISTER PACK
Product NDC 50804-120
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Bisacodyl
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130416
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Good Sense (Geiss, Destin & Dunn, Inc.)
Substance Name BISACODYL
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of womens laxative


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