FdaApplication
ANDA 203662
Identifiers
- fda_app_no: ANDA203662
Properties
| Property | Value |
|---|---|
| applicant_name | HIKMA FARMACEUTICA PORTUGAL SA |
| application_type | ANDA |
| approval_date | 2018-11-07 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NOREPINEPHRINE BITARTRATE | NOREPINEPHRINE BITARTRATE | EQ 1MG BASE/ML | INJECTABLE;INJECTION |
1 product