FdaApplication
ANDA 062390
Identifiers
- fda_app_no: ANDA062390
Properties
| Property | Value |
|---|---|
| applicant_name | APOTHECON INC DIV BRISTOL MYERS SQUIBB |
| application_type | ANDA |
| approval_date | 1982-06-10 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ULTRACEF | CEFADROXIL/CEFADROXIL HEMIHYDRATE | EQ 1GM BASE | TABLET;ORAL |
1 product