FdaApplication
ANDA 212822
Identifiers
- fda_app_no: ANDA212822
Properties
| Property | Value |
|---|---|
| applicant_name | HUONS CO LTD |
| application_type | ANDA |
| approval_date | 2019-12-30 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| BUPIVACAINE HYDROCHLORIDE | BUPIVACAINE HYDROCHLORIDE | 0.75% | INJECTABLE;SPINAL |
1 product