# Mycophenolate Mofetil

NDC: 67877-225
Generic name: Mycophenolate Mofetil
Labeler / Manufacturer: Ascend Laboratories, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20111128

FDA application: ANDA091249

## Active ingredients

- MYCOPHENOLATE MOFETIL: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"67877-225"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67877-225
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9f84ea84-2d8b-4d91-a33f-7dfb5df937dc