KIKKOMAN BIOCHEMIFA CO

Overview

KIKKOMAN BIOCHEMIFA CO is an active pharmaceutical ingredient (API) supplier with 2 active FDA Type II Drug Master Files, covering SODIUM HYALURONATE OF PHARMACEUTICAL GRADE; SODIUM HYALURONATE PHARMACEUTICAL GS GRADE.

API / Drug Master Files

KIKKOMAN BIOCHEMIFA CO holds 2 active (2 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 HYALURONATE PHARMACEUTICAL GS GRADEActive2019-03-18
• SODIUM HYALURONATE OF PHARMACEUTICAL GRADEActive1997-10-01

FDA compliance signals

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