Compare the 2 manufacturers holding an active US Drug Master File for Nesiritide API, with DMF numbers and filing years from the FDA's quarterly DMF list.
Directory listing last reviewed October 2026.
2 manufacturers hold an active Type II Drug Master File for NesiritideAPI, 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.
| Manufacturer | Location | US DMF | Filed |
|---|---|---|---|
| BCN Peptides | Spain (Barcelona) | 26676 | 2012 |
| Hybio Pharmaceutical | China | 27265 | 2013 |
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