DANIPHARM AS

Overview

DANIPHARM AS is an active pharmaceutical ingredient (API) supplier with 1 active FDA Type II Drug Master File, covering LACTULOSE CONCENTRATE.

API / Drug Master Files

DANIPHARM AS holds 1 active (2 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.

• LACTULOSE CONCENTRATEActive1990-09-20
• LACTULOSE PURUM LIQUIDUMInactive2005-06-01

FDA compliance signals

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