Product NDC: | 55154-1327 |
Proprietary Name: | Senna |
Non Proprietary Name: | Sennosides |
Active Ingredient(s): | 8.6 mg/1 & nbsp; Sennosides |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55154-1327 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20110602 |
Package NDC: | 55154-1327-9 |
Package Description: | 6 BLISTER PACK in 1 CARTON (55154-1327-9) > 5 TABLET in 1 BLISTER PACK |
NDC Code | 55154-1327-9 |
Proprietary Name | Senna |
Package Description | 6 BLISTER PACK in 1 CARTON (55154-1327-9) > 5 TABLET in 1 BLISTER PACK |
Product NDC | 55154-1327 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Sennosides |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20110602 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Cardinal Health |
Substance Name | SENNOSIDES |
Strength Number | 8.6 |
Strength Unit | mg/1 |
Pharmaceutical Classes |