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Senna Plus
Senna Plus - 21695-722-00 - (Senna Plus)
Drug Information of Senna Plus
| Product NDC: | 21695-722 |
| Proprietary Name: | Senna Plus |
| Non Proprietary Name: | Senna Plus |
| Active Ingredient(s): | 8.6 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: | 21695-722 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090710 |
Package Information of Senna Plus
| Package NDC: | 21695-722-00 |
| Package Description: | 100 TABLET in 1 BOTTLE (21695-722-00) |
NDC Information of Senna Plus
| NDC Code | 21695-722-00 |
| Proprietary Name | Senna Plus |
| Package Description | 100 TABLET in 1 BOTTLE (21695-722-00) |
| Product NDC | 21695-722 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Senna Plus |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090710 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | SENNOSIDES A AND B |
| Strength Number | 8.6 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
