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) |
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 NDC: | 67618-311-60 |
Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (67618-311-60) > 60 TABLET in 1 BOTTLE, PLASTIC |
NDC Code | 67618-311-60 |
Proprietary Name | Senokot-S |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (67618-311-60) > 60 TABLET in 1 BOTTLE, PLASTIC |
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 |