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Bisacodyl
Bisacodyl - 24236-199-30 - (Bisacodyl)
Drug Information of Bisacodyl
| Product NDC: | 24236-199 |
| 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: | 24236-199 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075659 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100804 |
Package Information of Bisacodyl
| Package NDC: | 24236-199-30 |
| Package Description: | 400 TABLET in 1 CANISTER (24236-199-30) |
NDC Information of Bisacodyl
| NDC Code | 24236-199-30 |
| Proprietary Name | Bisacodyl |
| Package Description | 400 TABLET in 1 CANISTER (24236-199-30) |
| Product NDC | 24236-199 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Bisacodyl |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100804 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | BISACODYL |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Increased Large Intestinal Motility [PE],Stimulant Laxative [EPC],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE] |
