Dulcolax - 0597-0012-38 - (bisacodyl)

Alphabetical Index


Drug Information of Dulcolax

Product NDC: 0597-0012
Proprietary Name: Dulcolax
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 Dulcolax

Product NDC: 0597-0012
Labeler Name: Boehringer Ingelheim Pharmaceuticals, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part334
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20011001

Package Information of Dulcolax

Package NDC: 0597-0012-38
Package Description: 1 BLISTER PACK in 1 CARTON (0597-0012-38) > 8 TABLET, COATED in 1 BLISTER PACK

NDC Information of Dulcolax

NDC Code 0597-0012-38
Proprietary Name Dulcolax
Package Description 1 BLISTER PACK in 1 CARTON (0597-0012-38) > 8 TABLET, COATED in 1 BLISTER PACK
Product NDC 0597-0012
Product Type Name HUMAN OTC DRUG
Non Proprietary Name bisacodyl
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20011001
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Boehringer Ingelheim Pharmaceuticals, Inc.
Substance Name BISACODYL
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Dulcolax


General Information