SEIKAGAKU CORP
Overview
SEIKAGAKU CORP is an active pharmaceutical ingredient (API) supplier with 1 active FDA Type II Drug Master File, covering SODIUM CHONDROITIN SULFATE (N).
Core services & business areas
Active pharmaceutical ingredients supplied
Substances SEIKAGAKU CORP 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
SEIKAGAKU CORP holds 1 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.
- SODIUM CHONDROITIN SULFATE (N)Active2018-10-31
- SODIUM HYALURONATEInactive2011-11-28
- SODIUM CHONDROITIN SULFATE (N)Inactive2008-04-10
- SODIUM CHONDROITIN SULFATE "SEIKAGAKU" FOR INJECTIONInactive2007-03-02
FDA compliance signals
No FDA recalls, Warning Letters, or Form 483 observations are linked to SEIKAGAKU CORP in our records. PharmaTek screens the full directory against live FDA enforcement data.
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