FdaApplication
ANDA 203619
Identifiers
- fda_app_no: ANDA203619
Properties
| Property | Value |
|---|---|
| applicant_name | HIKMA PHARMS |
| application_type | ANDA |
| approval_date | 2017-11-13 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PENTOBARBITAL SODIUM | PENTOBARBITAL SODIUM | 50MG/ML | INJECTABLE;INJECTION |
1 product