| Product NDC: | 50804-190 |
| Proprietary Name: | Bisacodyl 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: | 50804-190 |
| Labeler Name: | Geiss, Destin & Dunn, Inc (Goodsense) |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100716 |
| Package NDC: | 50804-190-03 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (50804-190-03) > 25 TABLET, COATED in 1 BLISTER PACK |
| NDC Code | 50804-190-03 |
| Proprietary Name | Bisacodyl Laxative |
| Package Description | 1 BLISTER PACK in 1 CARTON (50804-190-03) > 25 TABLET, COATED in 1 BLISTER PACK |
| Product NDC | 50804-190 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Bisacodyl |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100716 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Geiss, Destin & Dunn, Inc (Goodsense) |
| Substance Name | BISACODYL |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |