Product NDC: | 49483-046 |
Proprietary Name: | NEW CORRECT |
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: | 49483-046 |
Labeler Name: | Time-Cap Labs, Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part334 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20080806 |
Package NDC: | 49483-046-00 |
Package Description: | 100000 TABLET, DELAYED RELEASE in 1 CARTON (49483-046-00) |
NDC Code | 49483-046-00 |
Proprietary Name | NEW CORRECT |
Package Description | 100000 TABLET, DELAYED RELEASE in 1 CARTON (49483-046-00) |
Product NDC | 49483-046 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | BISACODYL |
Dosage Form Name | TABLET, DELAYED RELEASE |
Route Name | ORAL |
Start Marketing Date | 20080806 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Time-Cap Labs, Inc |
Substance Name | BISACODYL |
Strength Number | 5 |
Strength Unit | mg/1 |
Pharmaceutical Classes |