Bisacodyl - 11534-013-01 - (Bisacodyl)

Alphabetical Index


Drug Information of Bisacodyl

Product NDC: 11534-013
Proprietary Name: Bisacodyl
Non Proprietary Name: Bisacodyl
Active Ingredient(s): 5    mg/1 & nbsp;   Bisacodyl
Administration Route(s): ORAL
Dosage Form(s): TABLET, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Bisacodyl

Product NDC: 11534-013
Labeler Name: Sunrise Pharmaceutical Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part334
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20050708

Package Information of Bisacodyl

Package NDC: 11534-013-01
Package Description: 100 TABLET, DELAYED RELEASE in 1 BOTTLE (11534-013-01)

NDC Information of Bisacodyl

NDC Code 11534-013-01
Proprietary Name Bisacodyl
Package Description 100 TABLET, DELAYED RELEASE in 1 BOTTLE (11534-013-01)
Product NDC 11534-013
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Bisacodyl
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20050708
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Sunrise Pharmaceutical Inc
Substance Name BISACODYL
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Bisacodyl


General Information