MARUHA NICHIRO CORP

Overview

MARUHA NICHIRO CORP is an active pharmaceutical ingredient (API) supplier with 1 active FDA Type II Drug Master File, covering SODIUM HYALURONATE FH AND SODIUM HYALURONATE FL.

API / Drug Master Files

MARUHA NICHIRO CORP 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.

• SODIUM HYALURONATE FH AND SODIUM HYALURONATE FLActive2011-03-10

FDA compliance signals

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