# Mycophenolate Mofetil

NDC: 71288-803
Generic name: Mycophenolate Mofetil
Labeler / Manufacturer: Meitheal Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20210115

FDA application: ANDA212130

## Active ingredients

- MYCOPHENOLATE MOFETIL: 500 mg/20mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71288-803"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71288-803
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9650af9b-d36f-4a2f-9647-d0f798933402