Overview
BK GIULINI GMBH is an active pharmaceutical ingredient (API) supplier with 1 active FDA Type II Drug Master File, covering PHOSKADENT NA 211 (SODIUM MONOFLUOROPHOSPHATE).
API / Drug Master Files
BK GIULINI GMBH 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.
- PHOSKADENT NA 211 (SODIUM MONOFLUOROPHOSPHATE)Active1987-04-07
- SUCRALFATE POWDERInactive1996-02-28
FDA compliance signals
No FDA recalls, Warning Letters, or Form 483 observations are linked to BK GIULINI GMBH in our records. PharmaTek screens the full directory against live FDA enforcement data.
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