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Nitetime Cough
Nitetime Cough - 41250-668-40 - (Dextromethorphan Hydrobromide, Doxylamine Succinate)
Drug Information of Nitetime Cough
| Product NDC: | 41250-668 |
| 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) |
Labeler Information of Nitetime Cough
| Product NDC: | 41250-668 |
| Labeler Name: | Meijer Distribution Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20030303 |
Package Information of Nitetime Cough
| Package NDC: | 41250-668-40 |
| Package Description: | 355 mL in 1 BOTTLE (41250-668-40) |
NDC Information of Nitetime Cough
| NDC Code | 41250-668-40 |
| Proprietary Name | Nitetime Cough |
| Package Description | 355 mL in 1 BOTTLE (41250-668-40) |
| Product NDC | 41250-668 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dextromethorphan Hydrobromide, Doxylamine Succinate |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20030303 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Meijer Distribution Inc |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE |
| Strength Number | 30; 12.5 |
| Strength Unit | mg/30mL; mg/30mL |
| Pharmaceutical Classes |
