FdaApplication
ANDA 077838
Identifiers
- fda_app_no: ANDA077838
Properties
| Property | Value |
|---|---|
| applicant_name | HIKMA FARMACEUTICA PORTUGAL SA |
| application_type | ANDA |
| approval_date | 2023-01-17 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| BETAMETHASONE ACETATE AND BETAMETHASONE SODIUM PHOSPHATE | BETAMETHASONE ACETATE; BETAMETHASONE SODIUM PHOSPHATE | 3MG/ML;EQ 3MG BASE/ML | INJECTABLE;INJECTION |
1 product