Overview

SIOUX PHARM INC is an active pharmaceutical ingredient (API) supplier with 1 active FDA Type II Drug Master File, covering CHONDROITIN SULFATE SODIUM USP.

API / Drug Master Files

SIOUX PHARM INC 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.

  • CHONDROITIN SULFATE SODIUM USPActive1999-08-26

FDA compliance signals

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

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