FdaApplication
NDA 212319
Identifiers
- fda_app_no: NDA212319
Properties
| Property | Value |
|---|---|
| applicant_name | RAFA LABORATORIES LTD |
| application_type | NDA |
| approval_date | 2018-07-09 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ATROPINE (AUTOINJECTOR) | ATROPINE | EQ 2MG SULFATE/0.7ML (EQ 2MG SULFATE/0.7ML) | SOLUTION;INTRAMUSCULAR |
1 product