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Bisacodyl
Bisacodyl - 50730-1016-0 - (bisacodyl)
Drug Information of Bisacodyl
| Product NDC: | 50730-1016 |
| Proprietary Name: | Bisacodyl |
| Non Proprietary Name: | bisacodyl |
| Active Ingredient(s): | 10 mg/1 & nbsp; bisacodyl |
| Administration Route(s): | RECTAL |
| Dosage Form(s): | SUPPOSITORY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Bisacodyl
| Product NDC: | 50730-1016 |
| Labeler Name: | H and P Industries, Inc. dba Triad Group |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090101 |
Package Information of Bisacodyl
| Package NDC: | 50730-1016-0 |
| Package Description: | 16 SUPPOSITORY in 1 BOX (50730-1016-0) |
NDC Information of Bisacodyl
| NDC Code | 50730-1016-0 |
| Proprietary Name | Bisacodyl |
| Package Description | 16 SUPPOSITORY in 1 BOX (50730-1016-0) |
| Product NDC | 50730-1016 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | bisacodyl |
| Dosage Form Name | SUPPOSITORY |
| Route Name | RECTAL |
| Start Marketing Date | 20090101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | H and P Industries, Inc. dba Triad Group |
| Substance Name | BISACODYL |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
