Senokot-S - 67618-311-01 - (standardized senna concentrate and docusate sodium)

Alphabetical Index


Drug Information of Senokot-S

Product NDC: 67618-311
Proprietary Name: Senokot-S
Non Proprietary Name: standardized senna concentrate and docusate sodium
Active Ingredient(s): 50; 8.6    mg/1; mg/1 & nbsp;   standardized senna concentrate and docusate sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Senokot-S

Product NDC: 67618-311
Labeler Name: Purdue Products LP
Product Type: HUMAN OTC DRUG
FDA Application Number: part334
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 19741001

Package Information of Senokot-S

Package NDC: 67618-311-01
Package Description: 1 BLISTER PACK in 1 CARTON (67618-311-01) > 10 TABLET in 1 BLISTER PACK

NDC Information of Senokot-S

NDC Code 67618-311-01
Proprietary Name Senokot-S
Package Description 1 BLISTER PACK in 1 CARTON (67618-311-01) > 10 TABLET in 1 BLISTER PACK
Product NDC 67618-311
Product Type Name HUMAN OTC DRUG
Non Proprietary Name standardized senna concentrate and docusate sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19741001
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Purdue Products LP
Substance Name DOCUSATE SODIUM; SENNOSIDES
Strength Number 50; 8.6
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Senokot-S


General Information