Overview

ABIONYX PHARMA is an active pharmaceutical ingredient (API) supplier with 1 active FDA Type II Drug Master File, covering NP-0730-PP DRUG SUBSTANCE.

API / Drug Master Files

ABIONYX PHARMA 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.

  • NP-0730-PP DRUG SUBSTANCEActive2007-09-04

FDA compliance signals

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

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