FdaApplication
NDA 019401
Identifiers
- fda_app_no: NDA019401
Properties
| Property | Value |
|---|---|
| applicant_name | UCB INC |
| application_type | NDA |
| approval_date | 1987-06-19 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PSEUDO-12 | PSEUDOEPHEDRINE POLISTIREX | EQ 60MG HYDROCHLORIDE/5ML | SUSPENSION, EXTENDED RELEASE;ORAL |
1 product