FdaApplication
ANDA 201751
Identifiers
- fda_app_no: ANDA201751
Properties
| Property | Value |
|---|---|
| applicant_name | HANSAMED INC |
| application_type | ANDA |
| approval_date | 2017-07-11 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ULTACAN | ARTICAINE HYDROCHLORIDE; EPINEPHRINE BITARTRATE | 4%;EQ 0.0085MG BASE/1.7ML (4% | INJECTABLE;INJECTION |
1 product