Senna-S - 61715-019-60 - (Sennosides and Docusate Sodium)

Alphabetical Index


Drug Information of Senna-S

Product NDC: 61715-019
Proprietary Name: Senna-S
Non Proprietary Name: Sennosides and Docusate Sodium
Active Ingredient(s): 50; 8.6    mg/1; mg/1 & nbsp;   Sennosides and Docusate Sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Senna-S

Product NDC: 61715-019
Labeler Name: Kinray Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part334
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110510

Package Information of Senna-S

Package NDC: 61715-019-60
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (61715-019-60) > 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

NDC Information of Senna-S

NDC Code 61715-019-60
Proprietary Name Senna-S
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (61715-019-60) > 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product NDC 61715-019
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Sennosides and Docusate Sodium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110510
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Kinray Inc.
Substance Name DOCUSATE SODIUM; SENNOSIDES
Strength Number 50; 8.6
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Senna-S


General Information