| 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 |