KYFORA BIO LLC
Overview
KYFORA BIO LLC is an active pharmaceutical ingredient (API) supplier with 1 active FDA Type II Drug Master File, covering POLY(ETHYLENEIMINE).
API / Drug Master Files
KYFORA BIO LLC holds 1 active (1 total) FDA Type II Drug Master File — 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.
- POLY(ETHYLENEIMINE)Active2025-03-14
FDA compliance signals
No FDA recalls, Warning Letters, or Form 483 observations are linked to KYFORA BIO LLC in our records. PharmaTek screens the full directory against live FDA enforcement data.
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