Compare the 12 manufacturers holding an active US Drug Master File for Lanreotide API, with DMF numbers and filing years from the FDA's quarterly DMF list.
Directory listing last reviewed October 2026.
12 manufacturers hold an active Type II Drug Master File for LanreotideAPI, taken from the FDA's quarterly DMF list; 10 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 |
|---|---|---|---|
| ALP Pharm Beijing | China (Beijing) | 24378 | 2010 |
| Sinopep Biopharma | China | 29693 | 2016 |
| Bachem Holding AG | Switzerland / USA | 33336 | 2019 |
| Sun Pharmaceutical IndustriesFDA import alert | India (Mumbai) | 36547 | 2023 |
| BCN Peptides | Spain (Barcelona) | 39254 | 2023 |
| Chengdu Shengnuo BiopharmFDA import alert | China | 39673 | 2024 |
| Dr. Reddy's Laboratories | India | 39768 | 2024 |
| Sichuan Duorui Biopharmaceutical | China (Chengdu) | 41446 | 2025 |
| Piramal Pharma Solutions | India (Mumbai) | 42310 | 2025 |
| Reliance Life SciencesFDA import alert | India (Navi Mumbai) | 42130 | 2025 |
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 Frontier Biopharmaceutical Co Ltd | 39483 | 2024 |
| Sichuan Huiyu Pharmaceutical Co Ltd | 42318 | 2025 |
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