Product NDC: | 0904-5165 |
Proprietary Name: | Senna-Lax |
Non Proprietary Name: | SENNOSIDES A AND B |
Active Ingredient(s): | 8.6 mg/1 & nbsp; SENNOSIDES A AND B |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0904-5165 |
Labeler Name: | Major Pharmaceuticals |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part334 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110504 |
Package NDC: | 0904-5165-61 |
Package Description: | 10 BLISTER PACK in 1 BOX (0904-5165-61) > 10 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Code | 0904-5165-61 |
Proprietary Name | Senna-Lax |
Package Description | 10 BLISTER PACK in 1 BOX (0904-5165-61) > 10 TABLET, FILM COATED in 1 BLISTER PACK |
Product NDC | 0904-5165 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | SENNOSIDES A AND B |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20110504 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Major Pharmaceuticals |
Substance Name | SENNOSIDES A AND B |
Strength Number | 8.6 |
Strength Unit | mg/1 |
Pharmaceutical Classes |