Home
>
National Drug Code (NDC)
>
Bisacodyl
Bisacodyl - 55154-3388-9 - (Bisacodyl)
Drug Information of Bisacodyl
| Product NDC: | 55154-3388 |
| Proprietary Name: | Bisacodyl |
| Non Proprietary Name: | Bisacodyl |
| Active Ingredient(s): | 5 mg/1 & nbsp; Bisacodyl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Bisacodyl
| Product NDC: | 55154-3388 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110602 |
Package Information of Bisacodyl
| Package NDC: | 55154-3388-9 |
| Package Description: | 30 TABLET in 1 BLISTER PACK (55154-3388-9) |
NDC Information of Bisacodyl
| NDC Code | 55154-3388-9 |
| Proprietary Name | Bisacodyl |
| Package Description | 30 TABLET in 1 BLISTER PACK (55154-3388-9) |
| Product NDC | 55154-3388 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Bisacodyl |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110602 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Cardinal Health |
| Substance Name | BISACODYL |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
