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SenokotXTRA
SenokotXTRA - 67618-315-36 - (standardized senna concentrate)
Drug Information of SenokotXTRA
| Product NDC: | 67618-315 |
| Proprietary Name: | SenokotXTRA |
| Non Proprietary Name: | standardized senna concentrate |
| Active Ingredient(s): | 17.2 mg/1 & nbsp; standardized senna concentrate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SenokotXTRA
| Product NDC: | 67618-315 |
| Labeler Name: | Purdue Products LP |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19880901 |
Package Information of SenokotXTRA
| Package NDC: | 67618-315-36 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (67618-315-36) > 12 TABLET in 1 BLISTER PACK |
NDC Information of SenokotXTRA
| NDC Code | 67618-315-36 |
| Proprietary Name | SenokotXTRA |
| Package Description | 3 BLISTER PACK in 1 CARTON (67618-315-36) > 12 TABLET in 1 BLISTER PACK |
| Product NDC | 67618-315 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | standardized senna concentrate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19880901 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Purdue Products LP |
| Substance Name | SENNOSIDES |
| Strength Number | 17.2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
