FdaApplication
ANDA 070071
Identifiers
- fda_app_no: ANDA070071
Properties
| Property | Value |
|---|---|
| applicant_name | ABRAXIS PHARMACEUTICAL PRODUCTS |
| application_type | ANDA |
| approval_date | 1984-12-03 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| METRONIDAZOLE | METRONIDAZOLE | 500MG/100ML | INJECTABLE;INJECTION |
1 product