FdaApplication
NDA 019090
Identifiers
- fda_app_no: NDA019090
Properties
| Property | Value |
|---|---|
| applicant_name | PAI HOLDINGS LLC DBA PHARMACEUTICAL ASSOCIATES INC |
| application_type | NDA |
| approval_date | 1984-10-19 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ZANTAC | RANITIDINE HYDROCHLORIDE | EQ 25MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION |
1 product