Product NDC: | 37205-779 |
Proprietary Name: | Leader Nite Time Cold Flu Relief |
Non Proprietary Name: | acetaminophen, dextromethorphan hydrobromide, doxylamine succinate |
Active Ingredient(s): | 500; 15; 6.25 mg/15mL; mg/15mL; mg/15mL & nbsp; acetaminophen, dextromethorphan hydrobromide, doxylamine succinate |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 37205-779 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20060620 |
Package NDC: | 37205-779-37 |
Package Description: | 177 mL in 1 BOTTLE (37205-779-37) |
NDC Code | 37205-779-37 |
Proprietary Name | Leader Nite Time Cold Flu Relief |
Package Description | 177 mL in 1 BOTTLE (37205-779-37) |
Product NDC | 37205-779 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | acetaminophen, dextromethorphan hydrobromide, doxylamine succinate |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20060620 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Cardinal Health |
Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE |
Strength Number | 500; 15; 6.25 |
Strength Unit | mg/15mL; mg/15mL; mg/15mL |
Pharmaceutical Classes |