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SENNA
SENNA - 65437-087-50 - (SENNA)
Drug Information of SENNA
| Product NDC: | 65437-087 |
| Proprietary Name: | SENNA |
| Non Proprietary Name: | SENNA |
| Active Ingredient(s): | 8.6 mg/1 & nbsp; SENNA |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SENNA
| Product NDC: | 65437-087 |
| Labeler Name: | HIMPRIT PHARMACHEM PVT LTD |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20091120 |
Package Information of SENNA
| Package NDC: | 65437-087-50 |
| Package Description: | 1 BAG in 1 DRUM (65437-087-50) > 50000 TABLET, FILM COATED in 1 BAG |
NDC Information of SENNA
| NDC Code | 65437-087-50 |
| Proprietary Name | SENNA |
| Package Description | 1 BAG in 1 DRUM (65437-087-50) > 50000 TABLET, FILM COATED in 1 BAG |
| Product NDC | 65437-087 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SENNA |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20091120 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | HIMPRIT PHARMACHEM PVT LTD |
| Substance Name | SENNA |
| Strength Number | 8.6 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
