# Mycophenolate Mofetil

NDC: 70752-294
Generic name: Mycophenolate Mofetil
Labeler / Manufacturer: QUAGEN PHARMACEUTICALS LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SUSPENSION
Routes: ORAL
Marketing started: 20260806

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:"70752-294"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70752-294
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=838449b3-4397-4e35-b9b9-683f5a48bff2