| Product NDC: | 63941-072 |
| Proprietary Name: | Night Time Cough |
| Non Proprietary Name: | DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE |
| Active Ingredient(s): | 15; 135 mg/15mL; mg/5mL & nbsp; DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 63941-072 |
| Labeler Name: | Best Choice |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100107 |
| Package NDC: | 63941-072-06 |
| Package Description: | 177 mL in 1 BOTTLE, PLASTIC (63941-072-06) |
| NDC Code | 63941-072-06 |
| Proprietary Name | Night Time Cough |
| Package Description | 177 mL in 1 BOTTLE, PLASTIC (63941-072-06) |
| Product NDC | 63941-072 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20100107 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Best Choice |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE |
| Strength Number | 15; 135 |
| Strength Unit | mg/15mL; mg/5mL |
| Pharmaceutical Classes |