GUAIFENESIN AND DEXTROMETHORPHAN HYDROBROMIDE (DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENES) — FDA Approval ANDA214781 (SUN PHARM)
GUAIFENESIN AND DEXTROMETHORPHAN HYDROBROMIDE (DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENES) — FDA Approval ANDA214781 (SUN PHARM) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: GUAIFENESIN AND DEXTROMETHORPHAN HYDROBROMIDE; Active ingredients: DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENE
| Brand name | GUAIFENESIN AND DEXTROMETHORPHAN HYDROBROMIDE |
|---|---|
| Active ingredients | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
| Application number | ANDA214781 |
| Sponsor | SUN PHARM |
| Dosage form | TABLET, EXTENDED RELEASE |
| Route | ORAL |
| Marketing status | Over-the-counter |
| Products in application | 2 |
| First approval date | 20210701 |
| Source | openFDA Drugs@FDA |
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