FdaApplication
NDA 201739
Identifiers
- fda_app_no: NDA201739
Properties
| Property | Value |
|---|---|
| applicant_name | KALEO INC |
| application_type | NDA |
| approval_date | 2012-08-10 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| AUVI-Q | EPINEPHRINE | EQ 0.15MG/DELIVERY | SOLUTION;INTRAMUSCULAR, SUBCUTANEOUS |
| AUVI-Q | EPINEPHRINE | EQ 0.3MG/DELIVERY | SOLUTION;INTRAMUSCULAR, SUBCUTANEOUS |
| AUVI-Q | EPINEPHRINE | EQ 0.1MG/DELIVERY | SOLUTION;INTRAMUSCULAR, SUBCUTANEOUS |
3 products