| Product NDC: | 65437-035 |
| Proprietary Name: | SENNA LEAF and DOCUSATE SODIUM |
| Non Proprietary Name: | SENNA LEAF and DOCUSATE SODIUM |
| Active Ingredient(s): | 50; 8.6 mg/1; mg/1 & nbsp; SENNA LEAF and DOCUSATE SODIUM |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 65437-035 |
| Labeler Name: | HIMPRIT PHARMACHEM PVT LTD |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100401 |
| Package NDC: | 65437-035-70 |
| Package Description: | 1 BAG in 1 DRUM (65437-035-70) > 75000 TABLET, FILM COATED in 1 BAG |
| NDC Code | 65437-035-70 |
| Proprietary Name | SENNA LEAF and DOCUSATE SODIUM |
| Package Description | 1 BAG in 1 DRUM (65437-035-70) > 75000 TABLET, FILM COATED in 1 BAG |
| Product NDC | 65437-035 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SENNA LEAF and DOCUSATE SODIUM |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100401 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | HIMPRIT PHARMACHEM PVT LTD |
| Substance Name | DOCUSATE SODIUM; SENNA LEAF |
| Strength Number | 50; 8.6 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |