Overview

PURISYS LLC is an active pharmaceutical ingredient (API) supplier with 7 active FDA Type II Drug Master Files, covering CANNABIDIOL DRUG SUBSTANCE; DEXMETHYLPHENIDATE HYDROCHLORIDE; DRONABINOL DRUG SUBSTANCE; DRONABINOL DRUG SUBSTANCE IN SESAME OIL; NABILONE DRUG SUBSTANCE; NALMEFENE HYDROCHLORIDE DRUG SUBSTANCE.

API / Drug Master Files

PURISYS LLC holds 7 active (8 total) FDA Type II Drug Master Files — identifying it as an active-substance / API supplier. Type II DMFs are filed with the FDA to support the use of an active pharmaceutical ingredient in drug applications.

  • NALMEFENE HYDROCHLORIDE DRUG SUBSTANCEActive2024-08-30
  • PSILOCYBINActive2023-01-31
  • DRONABINOL DRUG SUBSTANCEActive2021-10-12
  • NABILONE DRUG SUBSTANCEActive2020-12-15
  • CANNABIDIOL DRUG SUBSTANCEActive2019-02-22
  • DEXMETHYLPHENIDATE HYDROCHLORIDEActive2016-05-27
  • DRONABINOL DRUG SUBSTANCE IN SESAME OILActive2007-07-16
  • DRONABINOL, 10% IN SESAME OILInactive2006-04-07

FDA compliance signals

No FDA recalls, Warning Letters, or Form 483 observations are linked to PURISYS LLC in our records. PharmaTek screens the full directory against live FDA enforcement data.

Ready to Accelerate Your
Discovery Workflow?

Find, vet, and source drug-manufacturing partners faster — with FDA compliance screening built in. Start free for 14 days.