FdaApplication
NDA 019819
Identifiers
- fda_app_no: NDA019819
Properties
| Property | Value |
|---|---|
| applicant_name | YAMANOUCHI EUROPE BV |
| application_type | NDA |
| approval_date | 1988-09-15 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| LOCOID | HYDROCORTISONE BUTYRATE | 0.1% | SOLUTION;TOPICAL |
1 product