FdaApplication
NDA 020716
Identifiers
- fda_app_no: NDA020716
Properties
| Property | Value |
|---|---|
| applicant_name | ABBVIE INC |
| application_type | NDA |
| approval_date | 1997-09-23 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| VICOPROFEN | HYDROCODONE BITARTRATE; IBUPROFEN | 7.5MG;200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
1 product