Docuprene - 68788-9857-6 - (DOCUSATE SODIUM)

Alphabetical Index


Drug Information of Docuprene

Product NDC: 68788-9857
Proprietary Name: Docuprene
Non Proprietary Name: DOCUSATE SODIUM
Active Ingredient(s): 100    mg/1 & nbsp;   DOCUSATE SODIUM
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Docuprene

Product NDC: 68788-9857
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part334
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120312

Package Information of Docuprene

Package NDC: 68788-9857-6
Package Description: 60 TABLET in 1 BOTTLE (68788-9857-6)

NDC Information of Docuprene

NDC Code 68788-9857-6
Proprietary Name Docuprene
Package Description 60 TABLET in 1 BOTTLE (68788-9857-6)
Product NDC 68788-9857
Product Type Name HUMAN OTC DRUG
Non Proprietary Name DOCUSATE SODIUM
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120312
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Preferred Pharmaceuticals, Inc
Substance Name DOCUSATE SODIUM
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Docuprene


General Information