Product NDC: | 30142-668 |
Proprietary Name: | NiteTime Cough |
Non Proprietary Name: | Dextromethorphan Hydrobromide, Doxylamine Succinate |
Active Ingredient(s): | 30; 12.5 mg/30mL; mg/30mL & nbsp; Dextromethorphan Hydrobromide, Doxylamine Succinate |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 30142-668 |
Labeler Name: | Kroger Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20021120 |
Package NDC: | 30142-668-38 |
Package Description: | 295 mL in 1 BOTTLE (30142-668-38) |
NDC Code | 30142-668-38 |
Proprietary Name | NiteTime Cough |
Package Description | 295 mL in 1 BOTTLE (30142-668-38) |
Product NDC | 30142-668 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Dextromethorphan Hydrobromide, Doxylamine Succinate |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20021120 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Kroger Company |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE |
Strength Number | 30; 12.5 |
Strength Unit | mg/30mL; mg/30mL |
Pharmaceutical Classes |