FdaApplication
NDA 017463
Identifiers
- fda_app_no: NDA017463
Properties
| Property | Value |
|---|---|
| applicant_name | MCNEIL CONSUMER HEALTHCARE DIV MCNEIL PPC INC |
| application_type | NDA |
| approval_date | 1985-05-22 |
Products (4)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MOTRIN | IBUPROFEN | 800MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| MOTRIN | IBUPROFEN | 300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| MOTRIN | IBUPROFEN | 400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| MOTRIN | IBUPROFEN | 600MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
4 products