| Product NDC: | 65224-618 |
| Proprietary Name: | Z-COF 1 |
| Non Proprietary Name: | DEXTROMETHORPHAN HYDROBROMIDE, PSEUDOEPHEDRINE HYDROCHLORIDE, and GUAIFENESIN |
| Active Ingredient(s): | 15; 211; 30 mg/5mL; mg/5mL; mg/5mL & nbsp; DEXTROMETHORPHAN HYDROBROMIDE, PSEUDOEPHEDRINE HYDROCHLORIDE, and GUAIFENESIN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 65224-618 |
| Labeler Name: | Pernix Therapeutics, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110502 |
| Package NDC: | 65224-618-16 |
| Package Description: | 473 mL in 1 BOTTLE (65224-618-16) |
| NDC Code | 65224-618-16 |
| Proprietary Name | Z-COF 1 |
| Package Description | 473 mL in 1 BOTTLE (65224-618-16) |
| Product NDC | 65224-618 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DEXTROMETHORPHAN HYDROBROMIDE, PSEUDOEPHEDRINE HYDROCHLORIDE, and GUAIFENESIN |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20110502 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Pernix Therapeutics, LLC |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 15; 211; 30 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |