FDA warning letter · Drugs

Macsen Drugs

Issued · Posted by FDA

Selected passages from the FDA letter

Quoted FDA text from the published dataset. These selected excerpts are not the complete letter.

Passage 1

Failure of your quality unit to exercise its responsibility to ensure the API manufactured at your facility are in compliance with CGMP.

Passage 2

Failure of your quality unit to ensure that there is stability data to support retest or expiry dates and storage conditions of API.