FdaApplication
NDA 018917
Identifiers
- fda_app_no: NDA018917
Properties
| Property | Value |
|---|---|
| applicant_name | PROMIUS PHARMA LLC |
| application_type | NDA |
| approval_date | 1984-12-28 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SECTRAL | ACEBUTOLOL HYDROCHLORIDE | EQ 200MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | CAPSULE;ORAL |
| SECTRAL | ACEBUTOLOL HYDROCHLORIDE | EQ 400MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | CAPSULE;ORAL |
2 products