FdaApplication
NDA 021620
Identifiers
- fda_app_no: NDA021620
Properties
| Property | Value |
|---|---|
| applicant_name | RECKITT BENCKISER LLC |
| application_type | NDA |
| approval_date | 2004-04-29 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MUCINEX DM | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN | 30MG;600MG | TABLET, EXTENDED RELEASE;ORAL |
| MUCINEX DM | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN | 60MG;1.2GM | TABLET, EXTENDED RELEASE;ORAL |
2 products