FdaApplication
NDA 217338
Identifiers
- fda_app_no: NDA217338
Properties
| Property | Value |
|---|---|
| applicant_name | RECKITT BENCKISER LLC |
| application_type | NDA |
| approval_date | 2025-12-22 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MUCINEX 12HR COLD & FEVER MULTI-SYMPTOM | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; NAPROXEN SODIUM | 30MG;600MG;110MG | TABLET, EXTENDED RELEASE;ORAL |
1 product