# Mycophenolate Mofetil

NDC: 69238-1595
Generic name: Mycophenolate Mofetil
Labeler / Manufacturer: Amneal Pharmaceuticals NY LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SUSPENSION
Routes: ORAL
Marketing started: 20211105

FDA application: ANDA214871

## 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:"69238-1595"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69238-1595
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=27fd9381-8d82-4187-897f-98f41f94e90f