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Bisacodyl
Bisacodyl - 11534-013-25 - (Bisacodyl)
Drug Information of Bisacodyl
| Product NDC: | 11534-013 |
| Proprietary Name: | Bisacodyl |
| 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) |
Labeler Information of Bisacodyl
| Product NDC: | 11534-013 |
| Labeler Name: | Sunrise Pharmaceutical Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20050708 |
Package Information of Bisacodyl
| Package NDC: | 11534-013-25 |
| Package Description: | 25 TABLET, DELAYED RELEASE in 1 BOTTLE (11534-013-25) |
NDC Information of Bisacodyl
| NDC Code | 11534-013-25 |
| Proprietary Name | Bisacodyl |
| Package Description | 25 TABLET, DELAYED RELEASE in 1 BOTTLE (11534-013-25) |
| Product NDC | 11534-013 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Bisacodyl |
| Dosage Form Name | TABLET, DELAYED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20050708 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Sunrise Pharmaceutical Inc |
| Substance Name | BISACODYL |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
