FdaApplication
NDA 021712
Identifiers
- fda_app_no: NDA021712
Properties
| Property | Value |
|---|---|
| applicant_name | UCB INC |
| application_type | NDA |
| approval_date | 2004-09-24 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| FLUXID | FAMOTIDINE | 40MG | TABLET, ORALLY DISINTEGRATING;ORAL |
| FLUXID | FAMOTIDINE | 20MG | TABLET, ORALLY DISINTEGRATING;ORAL |
2 products