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Senokot
Senokot - 67618-300-10 - (standardized senna concentrate)
Drug Information of Senokot
| Product NDC: | 67618-300 |
| Proprietary Name: | Senokot |
| Non Proprietary Name: | standardized senna concentrate |
| Active Ingredient(s): | 8.6 mg/1 & nbsp; standardized senna concentrate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Senokot
| Product NDC: | 67618-300 |
| Labeler Name: | Purdue Products LP |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19560601 |
Package Information of Senokot
| Package NDC: | 67618-300-10 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (67618-300-10) > 100 TABLET in 1 BOTTLE, PLASTIC |
NDC Information of Senokot
| NDC Code | 67618-300-10 |
| Proprietary Name | Senokot |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (67618-300-10) > 100 TABLET in 1 BOTTLE, PLASTIC |
| Product NDC | 67618-300 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | standardized senna concentrate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19560601 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Purdue Products LP |
| Substance Name | SENNOSIDES |
| Strength Number | 8.6 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
