FdaApplication
ANDA 213641
Identifiers
- fda_app_no: ANDA213641
Properties
| Property | Value |
|---|---|
| applicant_name | AMPHASTAR PHARMACEUTICALS INC |
| application_type | ANDA |
| approval_date | 2025-12-12 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| TERIPARATIDE | TERIPARATIDE | 0.56MG/2.24ML (0.25MG/ML) | SOLUTION;SUBCUTANEOUS |
1 product