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Senna S
Senna S - 10267-0490-7 - (Sennosides and Sodium Dioctylsulfosuccinate)
Drug Information of Senna S
| Product NDC: | 10267-0490 |
| Proprietary Name: | Senna S |
| Non Proprietary Name: | Sennosides and Sodium Dioctylsulfosuccinate |
| Active Ingredient(s): | 50; 8.5 mg/1; mg/1 & nbsp; Sennosides and Sodium Dioctylsulfosuccinate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Senna S
| Product NDC: | 10267-0490 |
| Labeler Name: | Contract Pharmacal Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20010605 |
Package Information of Senna S
| Package NDC: | 10267-0490-7 |
| Package Description: | 60 TABLET in 1 BOTTLE (10267-0490-7) |
NDC Information of Senna S
| NDC Code | 10267-0490-7 |
| Proprietary Name | Senna S |
| Package Description | 60 TABLET in 1 BOTTLE (10267-0490-7) |
| Product NDC | 10267-0490 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sennosides and Sodium Dioctylsulfosuccinate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20010605 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Contract Pharmacal Corp |
| Substance Name | DOCUSATE SODIUM; SENNA LEAF |
| Strength Number | 50; 8.5 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
