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Senokot-S
Senokot-S - 67618-310-11 - (standardized senna concentrate and docusate sodium)
Drug Information of Senokot-S
| Product NDC: | 67618-310 |
| 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: | 67618-310 |
| 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: | 67618-310-11 |
| Package Description: | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (67618-310-11) > 10 TABLET in 1 BLISTER PACK |
NDC Information of Senokot-S
| NDC Code | 67618-310-11 |
| Proprietary Name | Senokot-S |
| Package Description | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (67618-310-11) > 10 TABLET in 1 BLISTER PACK |
| Product NDC | 67618-310 |
| 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 |
