UQUIFA ITALIA SPA
Overview
UQUIFA ITALIA SPA is an active pharmaceutical ingredient (API) supplier with 3 active FDA Type II Drug Master Files, covering CARISOPRODOL USP; PYRANTEL PAMOATE USP; PYRANTEL TARTRATE ZEOLEX.
Core services & business areas
Active pharmaceutical ingredients supplied
Substances UQUIFA ITALIA SPA is evidenced to supply (US FDA Drug Master File or EU CEP). Open any ingredient to see its full supplier landscape, CAS number and patent status.
API / Drug Master Files
UQUIFA ITALIA SPA holds 3 active (4 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.
- PYRANTEL TARTRATE ZEOLEXActive2007-01-04
- PYRANTEL PAMOATE USPActive2006-09-29
- CARISOPRODOL USPActive2004-06-03
- DOXYLAMINE SUCCINATE USPInactive2004-05-21
FDA compliance signals
No FDA recalls, Warning Letters, or Form 483 observations are linked to UQUIFA ITALIA SPA in our records. PharmaTek screens the full directory against live FDA enforcement data.
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