Compare the 1 manufacturers holding an active US Drug Master File for Pramlintide 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 PramlintideAPI, 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 Pramlintide API quotes| Manufacturer | Location | US DMF | Filed |
|---|---|---|---|
| Sun Pharmaceutical IndustriesFDA import alert | India (Mumbai) | 31548 | 2018 |
Request API quotes from several manufacturers at once. Compare other molecules on the peptide API manufacturers index.