MUCINEX DM (DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENES) — FDA Approval NDA021620 (RB HLTH)
MUCINEX DM (DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENES) — FDA Approval NDA021620 (RB HLTH) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: MUCINEX DM; Active ingredients: DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; Application number: NDA021620.
| Brand name | MUCINEX DM |
|---|---|
| Active ingredients | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
| Application number | NDA021620 |
| Sponsor | RB HLTH |
| Dosage form | TABLET, EXTENDED RELEASE |
| Route | ORAL |
| Marketing status | Over-the-counter |
| Products in application | 2 |
| First approval date | 20040429 |
| Source | openFDA Drugs@FDA |
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