Product NDC: | 16103-363 |
Proprietary Name: | Senna Tabs |
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) |
Product NDC: | 16103-363 |
Labeler Name: | Pharbest Pharmaceuticals, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part334 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20070124 |
Package NDC: | 16103-363-11 |
Package Description: | 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16103-363-11) |
NDC Code | 16103-363-11 |
Proprietary Name | Senna Tabs |
Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16103-363-11) |
Product NDC | 16103-363 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Senna |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20070124 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Pharbest Pharmaceuticals, Inc. |
Substance Name | SENNOSIDES A AND B |
Strength Number | 8.6 |
Strength Unit | mg/1 |
Pharmaceutical Classes |