FdaApplication
NDA 207768
Identifiers
- fda_app_no: NDA207768
Properties
| Property | Value |
|---|---|
| applicant_name | TRIS PHARMA INC |
| application_type | NDA |
| approval_date | 2015-04-30 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| TUZISTRA XR | CHLORPHENIRAMINE POLISTIREX; CODEINE POLISTIREX | EQ 2.8MG BASE/5ML;EQ 14.7MG BASE/5ML | SUSPENSION, EXTENDED RELEASE;ORAL |
1 product