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Senna Plus
Senna Plus - 68084-050-01 - (Senna Plus)
Drug Information of Senna Plus
| Product NDC: | 68084-050 |
| Proprietary Name: | Senna Plus |
| Non Proprietary Name: | Senna Plus |
| Active Ingredient(s): | 50; 8.6 ug/1; mg/1 & nbsp; Senna Plus |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Senna Plus
| Product NDC: | 68084-050 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100114 |
Package Information of Senna Plus
| Package NDC: | 68084-050-01 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (68084-050-01) > 10 TABLET in 1 BLISTER PACK (68084-050-11) |
NDC Information of Senna Plus
| NDC Code | 68084-050-01 |
| Proprietary Name | Senna Plus |
| Package Description | 10 BLISTER PACK in 1 CARTON (68084-050-01) > 10 TABLET in 1 BLISTER PACK (68084-050-11) |
| Product NDC | 68084-050 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Senna Plus |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100114 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | American Health Packaging |
| Substance Name | DOCUSATE SODIUM; SENNOSIDES |
| Strength Number | 50; 8.6 |
| Strength Unit | ug/1; mg/1 |
| Pharmaceutical Classes |
