Product NDC: | 63824-019 |
Proprietary Name: | Mucinex Fast-Max |
Non Proprietary Name: | dextromethorphan hydrobromide and guaifenesin |
Active Ingredient(s): | 20; 400 mg/20mL; mg/20mL & nbsp; dextromethorphan hydrobromide and guaifenesin |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63824-019 |
Labeler Name: | Reckitt Benckiser LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120718 |
Package NDC: | 63824-019-66 |
Package Description: | 180 mL in 1 BOTTLE (63824-019-66) |
NDC Code | 63824-019-66 |
Proprietary Name | Mucinex Fast-Max |
Package Description | 180 mL in 1 BOTTLE (63824-019-66) |
Product NDC | 63824-019 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | dextromethorphan hydrobromide and guaifenesin |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 20120718 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Reckitt Benckiser LLC |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
Strength Number | 20; 400 |
Strength Unit | mg/20mL; mg/20mL |
Pharmaceutical Classes |