Product NDC: | 55910-232 |
Proprietary Name: | Mucus Relief DM Max |
Non Proprietary Name: | Mucinex DM Max Maximum Strength |
Active Ingredient(s): | 20; 400 mg/20mL; mg/20mL & nbsp; Mucinex DM Max Maximum Strength |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55910-232 |
Labeler Name: | Dolgencorp, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20130101 |
Package NDC: | 55910-232-09 |
Package Description: | 266 mL in 1 BOTTLE, PLASTIC (55910-232-09) |
NDC Code | 55910-232-09 |
Proprietary Name | Mucus Relief DM Max |
Package Description | 266 mL in 1 BOTTLE, PLASTIC (55910-232-09) |
Product NDC | 55910-232 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Mucinex DM Max Maximum Strength |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20130101 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Dolgencorp, Inc. |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
Strength Number | 20; 400 |
Strength Unit | mg/20mL; mg/20mL |
Pharmaceutical Classes |