FdaApplication
ANDA 075650
Identifiers
- fda_app_no: ANDA075650
Properties
| Property | Value |
|---|---|
| applicant_name | ACTAVIS ELIZABETH LLC |
| application_type | ANDA |
| approval_date | 2001-09-14 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| FAMOTIDINE | FAMOTIDINE | 40MG | TABLET;ORAL |
| FAMOTIDINE | FAMOTIDINE | 20MG | TABLET;ORAL |
2 products