Product NDC: | 61715-039 |
Proprietary Name: | WOMENS GENTLE 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: | 61715-039 |
Labeler Name: | Preferred Plus (Kinray) |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part334 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100802 |
Package NDC: | 61715-039-30 |
Package Description: | 2 BLISTER PACK in 1 CARTON (61715-039-30) > 15 TABLET, COATED in 1 BLISTER PACK |
NDC Code | 61715-039-30 |
Proprietary Name | WOMENS GENTLE LAXATIVE |
Package Description | 2 BLISTER PACK in 1 CARTON (61715-039-30) > 15 TABLET, COATED in 1 BLISTER PACK |
Product NDC | 61715-039 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Bisacodyl |
Dosage Form Name | TABLET, COATED |
Route Name | ORAL |
Start Marketing Date | 20100802 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Preferred Plus (Kinray) |
Substance Name | BISACODYL |
Strength Number | 5 |
Strength Unit | mg/1 |
Pharmaceutical Classes |