DOK Plus - 55154-0733-0 - (DOK Plus)

Alphabetical Index


Drug Information of DOK Plus

Product NDC: 55154-0733
Proprietary Name: DOK Plus
Non Proprietary Name: DOK Plus
Active Ingredient(s): 50; 8.6    mg/1; mg/1 & nbsp;   DOK Plus
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of DOK Plus

Product NDC: 55154-0733
Labeler Name: Cardinal Health
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20110607

Package Information of DOK Plus

Package NDC: 55154-0733-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-0733-0) > 1 TABLET in 1 BLISTER PACK

NDC Information of DOK Plus

NDC Code 55154-0733-0
Proprietary Name DOK Plus
Package Description 10 BLISTER PACK in 1 BAG (55154-0733-0) > 1 TABLET in 1 BLISTER PACK
Product NDC 55154-0733
Product Type Name HUMAN OTC DRUG
Non Proprietary Name DOK Plus
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110607
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Cardinal Health
Substance Name DOCUSATE SODIUM; SENNOSIDES
Strength Number 50; 8.6
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of DOK Plus


General Information