Product NDC: | 42192-523 |
Proprietary Name: | Entre-Cough |
Non Proprietary Name: | Dextromethorphan Hydrobromide, Pseudoephedrine Hydrochloride, Guaifensin |
Active Ingredient(s): | 15; 175; 30 mg/5mL; mg/5mL; mg/5mL & nbsp; Dextromethorphan Hydrobromide, Pseudoephedrine Hydrochloride, Guaifensin |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 42192-523 |
Labeler Name: | Acella Pharmaceuticals, LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20130204 |
Package NDC: | 42192-523-16 |
Package Description: | 473 mL in 1 BOTTLE (42192-523-16) |
NDC Code | 42192-523-16 |
Proprietary Name | Entre-Cough |
Package Description | 473 mL in 1 BOTTLE (42192-523-16) |
Product NDC | 42192-523 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Dextromethorphan Hydrobromide, Pseudoephedrine Hydrochloride, Guaifensin |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20130204 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Acella Pharmaceuticals, LLC |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE |
Strength Number | 15; 175; 30 |
Strength Unit | mg/5mL; mg/5mL; mg/5mL |
Pharmaceutical Classes |