Product NDC: | 61715-038 |
Proprietary Name: | Stimulant Laxative |
Non Proprietary Name: | Bisacodyl |
Active Ingredient(s): | 5 mg/1 & nbsp; Bisacodyl |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 61715-038 |
Labeler Name: | Preferred Plus (Kinray) |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part334 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100713 |
Package NDC: | 61715-038-51 |
Package Description: | 100 TABLET, COATED in 1 BOTTLE, PLASTIC (61715-038-51) |
NDC Code | 61715-038-51 |
Proprietary Name | Stimulant Laxative |
Package Description | 100 TABLET, COATED in 1 BOTTLE, PLASTIC (61715-038-51) |
Product NDC | 61715-038 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Bisacodyl |
Dosage Form Name | TABLET, COATED |
Route Name | ORAL |
Start Marketing Date | 20100713 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Preferred Plus (Kinray) |
Substance Name | BISACODYL |
Strength Number | 5 |
Strength Unit | mg/1 |
Pharmaceutical Classes |