Overview
DSP is an active pharmaceutical ingredient (API) supplier with 3 active FDA Type II Drug Master Files, covering AMBERLITE IRP69; AMBERLITE IRP70; DUOLITE™ AP143/1083 CHOLESTYRAMINE RESIN USP.
API / Drug Master Files
DSP holds 3 active (3 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.
- AMBERLITE IRP70Active1998-04-24
- AMBERLITE IRP69Active1997-01-31
- DUOLITE™ AP143/1083 CHOLESTYRAMINE RESIN USPActive1984-12-10
FDA compliance signals
No FDA recalls, Warning Letters, or Form 483 observations are linked to DSP in our records. PharmaTek screens the full directory against live FDA enforcement data.
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