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In contrast, NAC 900 mg TID reduced FEV 1 decline (by 150 mL) versus placebo over 24 weeks, though primary endpoints were unmet due to underpowering (108)

What Did Not Change on July 23 No approved indication or dosing label exists The committee did not create an approved indication for ulcerative colitis, tendon injury, ligament injury, muscle recovery, joint pain, gut symptoms, or general wellness