| Product NDC: | 47682-889 |
| Proprietary Name: | Medique Medi-lax |
| Non Proprietary Name: | BISACODYL |
| Active Ingredient(s): | 5 mg/1 & nbsp; BISACODYL |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, DELAYED RELEASE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 47682-889 |
| Labeler Name: | Unifirst First Aid Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20081230 |
| Package NDC: | 47682-889-05 |
| Package Description: | 1 BLISTER PACK in 1 BOX (47682-889-05) > 25 TABLET, DELAYED RELEASE in 1 BLISTER PACK |
| NDC Code | 47682-889-05 |
| Proprietary Name | Medique Medi-lax |
| Package Description | 1 BLISTER PACK in 1 BOX (47682-889-05) > 25 TABLET, DELAYED RELEASE in 1 BLISTER PACK |
| Product NDC | 47682-889 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BISACODYL |
| Dosage Form Name | TABLET, DELAYED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20081230 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Unifirst First Aid Corporation |
| Substance Name | BISACODYL |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |