Dulcolax - 0597-0016-01 - (docusate sodium)

Alphabetical Index


Drug Information of Dulcolax

Product NDC: 0597-0016
Proprietary Name: Dulcolax
Non Proprietary Name: docusate sodium
Active Ingredient(s): 100    mg/1 & nbsp;   docusate sodium
Administration Route(s): ORAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Dulcolax

Product NDC: 0597-0016
Labeler Name: Boehringer Ingelheim Pharmaceuticals, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part334
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20021001

Package Information of Dulcolax

Package NDC: 0597-0016-01
Package Description: 100 GEL in 1 BOTTLE (0597-0016-01)

NDC Information of Dulcolax

NDC Code 0597-0016-01
Proprietary Name Dulcolax
Package Description 100 GEL in 1 BOTTLE (0597-0016-01)
Product NDC 0597-0016
Product Type Name HUMAN OTC DRUG
Non Proprietary Name docusate sodium
Dosage Form Name GEL
Route Name ORAL
Start Marketing Date 20021001
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Boehringer Ingelheim Pharmaceuticals, Inc.
Substance Name DOCUSATE SODIUM
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Dulcolax


General Information