# MYCOPHENOLATE MOFETIL

NDC: 72603-751
Generic name: mycophenolate mofetil
Labeler / Manufacturer: NorthStar Rx LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SUSPENSION
Routes: ORAL
Marketing started: 20260301

FDA application: ANDA218227

## Active ingredients

- MYCOPHENOLATE MOFETIL: 200 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72603-751"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72603-751
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=127eabe2-8386-452a-ad6b-d879e1f2c099