FdaApplication
NDA 019675
Identifiers
- fda_app_no: NDA019675
Properties
| Property | Value |
|---|---|
| applicant_name | GLAXO GROUP LTD ENGLAND DBA GLAXOSMITHKLINE |
| application_type | NDA |
| approval_date | 1988-12-30 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ZANTAC | RANITIDINE HYDROCHLORIDE | EQ 15MG BASE/ML | SYRUP;ORAL |
1 product