Product NDC: | 59640-072 |
Proprietary Name: | Night Time Cherry |
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: | 59640-072 |
Labeler Name: | H.E.B |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20090603 |
Package NDC: | 59640-072-01 |
Package Description: | 296 mL in 1 BOTTLE, PLASTIC (59640-072-01) |
NDC Code | 59640-072-01 |
Proprietary Name | Night Time Cherry |
Package Description | 296 mL in 1 BOTTLE, PLASTIC (59640-072-01) |
Product NDC | 59640-072 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20090603 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | H.E.B |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE |
Strength Number | 15; 135 |
Strength Unit | mg/15mL; mg/5mL |
Pharmaceutical Classes |