# Mycophenolate Mofetil

NDC: 0527-5160
Generic name: Mycophenolate Mofetil
Labeler / Manufacturer: Lannett Company, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SUSPENSION
Routes: ORAL
Marketing started: 20210729

FDA application: ANDA214525

## Active ingredients

- MYCOPHENOLATE MOFETIL: 200 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0527-5160"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0527-5160
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=24c0b94a-c141-44b6-a6f0-ade1669b254c