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 |