Home
>
National Drug Code (NDC)
>
Mucinex DM
Mucinex DM - 66715-9724-1 - (Guaifenesin and Dextromethorphan Hydrobromide)
Drug Information of Mucinex DM
| Product NDC: | 66715-9724 |
| Proprietary Name: | Mucinex DM |
| Non Proprietary Name: | Guaifenesin and Dextromethorphan Hydrobromide |
| Active Ingredient(s): | 30; 600 mg/1; mg/1 & nbsp; Guaifenesin and Dextromethorphan Hydrobromide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mucinex DM
| Product NDC: | 66715-9724 |
| Labeler Name: | Lil' Drug Store Products, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA021620 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100510 |
Package Information of Mucinex DM
| Package NDC: | 66715-9724-1 |
| Package Description: | 1 POUCH in 1 CARTON (66715-9724-1) > 2 TABLET in 1 POUCH |
NDC Information of Mucinex DM
| NDC Code | 66715-9724-1 |
| Proprietary Name | Mucinex DM |
| Package Description | 1 POUCH in 1 CARTON (66715-9724-1) > 2 TABLET in 1 POUCH |
| Product NDC | 66715-9724 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Guaifenesin and Dextromethorphan Hydrobromide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100510 |
| Marketing Category Name | NDA |
| Labeler Name | Lil' Drug Store Products, Inc. |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
| Strength Number | 30; 600 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
