# Mycophenolate Mofetil

NDC: 66689-307
Generic name: Mycophenolate Mofetil
Labeler / Manufacturer: VistaPharm, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SUSPENSION
Routes: ORAL
Marketing started: 20190215

FDA application: ANDA210370

## 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:"66689-307"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=66689-307
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=175d8b87-e06a-4c9e-b3de-378114b52274