FdaApplication
NDA 019111
Identifiers
- fda_app_no: NDA019111
Properties
| Property | Value |
|---|---|
| applicant_name | UCB INC |
| application_type | NDA |
| approval_date | 1987-12-31 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| TUSSIONEX PENNKINETIC | CHLORPHENIRAMINE POLISTIREX; HYDROCODONE POLISTIREX | EQ 8MG MALEATE/5ML;EQ 10MG BITARTRATE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SUSPENSION, EXTENDED RELEASE;ORAL |
1 product