# Mycophenolate Mofetil

NDC: 60687-494
Generic name: Mycophenolate Mofetil
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20200221
Marketing ended: 20260630
FDA application: ANDA065410

## Active ingredients

- MYCOPHENOLATE MOFETIL: 250 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60687-494"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60687-494
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=54e8bbc4-1f6b-4a15-8142-a8bac5ba8d49