FdaApplication
NDA 019885
Identifiers
- fda_app_no: NDA019885
Properties
| Property | Value |
|---|---|
| applicant_name | PFIZER PHARMACEUTICALS LTD |
| application_type | NDA |
| approval_date | 1991-11-19 |
Products (4)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ACCUPRIL | QUINAPRIL HYDROCHLORIDE | EQ 40MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| ACCUPRIL | QUINAPRIL HYDROCHLORIDE | EQ 20MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| ACCUPRIL | QUINAPRIL HYDROCHLORIDE | EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| ACCUPRIL | QUINAPRIL HYDROCHLORIDE | EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
4 products