FdaApplication
NDA 216359
Identifiers
- fda_app_no: NDA216359
Properties
| Property | Value |
|---|---|
| applicant_name | RAFA LABORATORIES LTD |
| application_type | NDA |
| approval_date | 2022-08-08 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MIDAZOLAM HYDROCHLORIDE (AUTOINJECTOR) | MIDAZOLAM HYDROCHLORIDE | EQ 10MG BASE/0.7ML (EQ 10MG BASE/0.7ML) | SOLUTION;INTRAMUSCULAR |
1 product