FdaApplication
ANDA 062376
Identifiers
- fda_app_no: ANDA062376
Properties
| Property | Value |
|---|---|
| applicant_name | BRISTOL LABORATORIES INC DIV BRISTOL MYERS CO |
| application_type | ANDA |
| approval_date | 1982-03-16 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ULTRACEF | CEFADROXIL/CEFADROXIL HEMIHYDRATE | EQ 250MG BASE/5ML | FOR SUSPENSION;ORAL |
| ULTRACEF | CEFADROXIL/CEFADROXIL HEMIHYDRATE | EQ 125MG BASE/5ML | FOR SUSPENSION;ORAL |
| ULTRACEF | CEFADROXIL/CEFADROXIL HEMIHYDRATE | EQ 500MG BASE/5ML | FOR SUSPENSION;ORAL |
3 products