FdaApplication
ANDA 063022
Identifiers
- fda_app_no: ANDA063022
Properties
| Property | Value |
|---|---|
| applicant_name | LOCH PHARMACEUTICALS INC |
| application_type | ANDA |
| approval_date | 1992-07-31 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| KANAMYCIN SULFATE | KANAMYCIN SULFATE | EQ 500MG BASE/2ML | INJECTABLE;INJECTION |
1 product