Product NDC: | 67510-0503 |
Proprietary Name: | Night Time Cough |
Non Proprietary Name: | Dextromethorphan HBr, Doxylamine succinate |
Active Ingredient(s): | 15; 6.25 mg/15mL; mg/15mL & nbsp; Dextromethorphan HBr, Doxylamine succinate |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67510-0503 |
Labeler Name: | Kareway Product, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120711 |
Package NDC: | 67510-0503-1 |
Package Description: | 295 mL in 1 BOTTLE (67510-0503-1) |
NDC Code | 67510-0503-1 |
Proprietary Name | Night Time Cough |
Package Description | 295 mL in 1 BOTTLE (67510-0503-1) |
Product NDC | 67510-0503 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Dextromethorphan HBr, Doxylamine succinate |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20120711 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Kareway Product, Inc. |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE |
Strength Number | 15; 6.25 |
Strength Unit | mg/15mL; mg/15mL |
Pharmaceutical Classes |