Product NDC: | 67510-0171 |
Proprietary Name: | Gentle Laxative |
Non Proprietary Name: | BIisacodyl |
Active Ingredient(s): | 5 mg/1 & nbsp; BIisacodyl |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67510-0171 |
Labeler Name: | Kareway Product, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part334 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120215 |
Package NDC: | 67510-0171-2 |
Package Description: | 2 BLISTER PACK in 1 BOX (67510-0171-2) > 10 TABLET, COATED in 1 BLISTER PACK |
NDC Code | 67510-0171-2 |
Proprietary Name | Gentle Laxative |
Package Description | 2 BLISTER PACK in 1 BOX (67510-0171-2) > 10 TABLET, COATED in 1 BLISTER PACK |
Product NDC | 67510-0171 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | BIisacodyl |
Dosage Form Name | TABLET, COATED |
Route Name | ORAL |
Start Marketing Date | 20120215 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Kareway Product, Inc. |
Substance Name | BISACODYL |
Strength Number | 5 |
Strength Unit | mg/1 |
Pharmaceutical Classes |