LIFECORE BIOMEDICAL LLC

Overview

LIFECORE BIOMEDICAL LLC is an active pharmaceutical ingredient (API) supplier with 1 active FDA Type II Drug Master File, covering SODIUM HYALURONATE.

API / Drug Master Files

LIFECORE BIOMEDICAL LLC holds 1 active (5 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 HYALURONATEActive1991-05-01
• SODIUM HYALURONATE, LSA-9850025 PROCESSInactive2014-11-17
• SODIUM HYALURONATE POWDER, SPECIFICATION LPD-9800037, PH 4.0 PROCESSInactive2012-02-03
• ANIMAL COMPONENT FREE SODIUM HYALURONATEInactive2007-10-26
• HY-50 HYALURONATE SODIUM STERILE INJECTIONInactive1995-07-25

FDA compliance signals

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