# Mycophenolate mofetil

NDC: 70518-2767
Generic name: Mycophenolate mofetil
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20200608

FDA application: ANDA090456

## Active ingredients

- MYCOPHENOLATE MOFETIL: 500 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-2767"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-2767
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=afb59492-2bb1-4cf1-af4b-a5020b56c124