FdaApplication
NDA 017920
Identifiers
- fda_app_no: NDA017920
Properties
| Property | Value |
|---|---|
| applicant_name | GLAXOSMITHKLINE |
| application_type | NDA |
| approval_date | 1983-12-14 |
Products (4)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| TAGAMET | CIMETIDINE | 400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| TAGAMET | CIMETIDINE | 800MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| TAGAMET | CIMETIDINE | 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| TAGAMET | CIMETIDINE | 300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
4 products