{"url_path":"/fda/drug/recalls/D-0734-2026","section_key":"summary","section_title":"DRUG Recall: MYLAN PHARMACEUTICALS INC — Mycophenolate Mofetil for Injection USP, 500 mg/Vial, Single Dose Vial, 4 vials per carton, Rx only, Manufactured for: Mylan Institutional LLC, Morgantown, WV, 26505 USA, Made in India, NDC 67457-386-00 (vial label) & NDC 67457-386-81 (carton label).","topic":"fda","document":{"doc_type":"drug-recall","doc_date":"2026-07-02","source_url":"https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0734-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"MYLAN PHARMACEUTICALS INC"},"word_count":73,"has_tables":false,"body_markdown":null}