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Mucus Relief DM
Mucus Relief DM - 50804-109-30 - (Dextromethorphan Hydrobromide and Guaifenesin)
Drug Information of Mucus Relief DM
| Product NDC: | 50804-109 |
| Proprietary Name: | Mucus Relief DM |
| Non Proprietary Name: | Dextromethorphan Hydrobromide and Guaifenesin |
| Active Ingredient(s): | 20; 400 mg/1; mg/1 & nbsp; Dextromethorphan Hydrobromide and Guaifenesin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mucus Relief DM
| Product NDC: | 50804-109 |
| Labeler Name: | Good Sense (Geiss, Destin & Dunn, Inc.) |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130430 |
Package Information of Mucus Relief DM
| Package NDC: | 50804-109-30 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 BOX (50804-109-30) > 30 TABLET, COATED in 1 BOTTLE, PLASTIC |
NDC Information of Mucus Relief DM
| NDC Code | 50804-109-30 |
| Proprietary Name | Mucus Relief DM |
| Package Description | 1 BOTTLE, PLASTIC in 1 BOX (50804-109-30) > 30 TABLET, COATED in 1 BOTTLE, PLASTIC |
| Product NDC | 50804-109 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dextromethorphan Hydrobromide and Guaifenesin |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20130430 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Good Sense (Geiss, Destin & Dunn, Inc.) |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
| Strength Number | 20; 400 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
