Compare the 2 manufacturers holding an active US Drug Master File for Atosiban 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 AtosibanAPI, taken from the FDA's quarterly DMF list; 1 of them are listed in this directory. 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 |
|---|---|---|---|
| Harbin Jixianglong BiotechFDA import alert | China (Harbin) | 39950 | 2024 |
Not yet listed in this directory, so we have not reviewed them. Names as printed in the FDA DMF list.
| DMF holder | US DMF | Filed |
|---|---|---|
| Sichuan Kelun Pharmaceutical Co Ltd | 44844 | 2026 |
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