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Night Relief Cough
Night Relief Cough - 55312-668-34 - (Dextromethorphan Hydrobromide, Doxylamine Succinate)
Drug Information of Night Relief Cough
| Product NDC: | 55312-668 |
| Proprietary Name: | Night Relief 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) |
Labeler Information of Night Relief Cough
| Product NDC: | 55312-668 |
| Labeler Name: | Western Family Foods Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20021021 |
Package Information of Night Relief Cough
| Package NDC: | 55312-668-34 |
| Package Description: | 237 mL in 1 BOTTLE (55312-668-34) |
NDC Information of Night Relief Cough
| NDC Code | 55312-668-34 |
| Proprietary Name | Night Relief Cough |
| Package Description | 237 mL in 1 BOTTLE (55312-668-34) |
| Product NDC | 55312-668 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dextromethorphan Hydrobromide, Doxylamine Succinate |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20021021 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Western Family Foods Inc |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE |
| Strength Number | 30; 12.5 |
| Strength Unit | mg/30mL; mg/30mL |
| Pharmaceutical Classes |
