Compare the 1 manufacturers holding an active US Drug Master File for Vosoritide API, with DMF numbers and filing years from the FDA's quarterly DMF list.
Directory listing last reviewed October 2026.
1 manufacturer holds an active Type II Drug Master File for VosoritideAPI, taken from the FDA's quarterly DMF list. A DMF lets a drug applicant reference the maker's manufacturing data. It is not an FDA approval. Check each manufacturer against the FDA import alert lists before ordering.
Request Vosoritide API quotes| Manufacturer | Location | US DMF | Filed |
|---|---|---|---|
| Apicore (RK Pharma) | USA (East Windsor, NJ) | 42084 | 2025 |
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