FdaApplication
NDA 020572
Identifiers
- fda_app_no: NDA020572
Properties
| Property | Value |
|---|---|
| applicant_name | HORIZON THERAPEUTICS US HOLDING LLC |
| application_type | NDA |
| approval_date | 1996-05-13 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| BUPHENYL | SODIUM PHENYLBUTYRATE | 500MG | TABLET;ORAL |
1 product