FdaApplication
ANDA 206224
Identifiers
- fda_app_no: ANDA206224
Properties
| Property | Value |
|---|---|
| applicant_name | LUOXIN AUROVITAS PHARMA CHENGDU CO LTD |
| application_type | ANDA |
| approval_date | 2017-10-17 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ALBUTEROL SULFATE | ALBUTEROL SULFATE | EQ 0.083% BASE | SOLUTION;INHALATION |
1 product