Product NDC: | 59640-098 |
Proprietary Name: | Tussin Cough Long Acting |
Non Proprietary Name: | DEXTROMETHORPHAN HYDROBROMIDE |
Active Ingredient(s): | 10 mg/5mL & nbsp; DEXTROMETHORPHAN HYDROBROMIDE |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59640-098 |
Labeler Name: | H.E.B |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100323 |
Package NDC: | 59640-098-08 |
Package Description: | 237 mL in 1 BOTTLE, PLASTIC (59640-098-08) |
NDC Code | 59640-098-08 |
Proprietary Name | Tussin Cough Long Acting |
Package Description | 237 mL in 1 BOTTLE, PLASTIC (59640-098-08) |
Product NDC | 59640-098 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | DEXTROMETHORPHAN HYDROBROMIDE |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20100323 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | H.E.B |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE |
Strength Number | 10 |
Strength Unit | mg/5mL |
Pharmaceutical Classes |