# Mycophenolate mofetil

NDC: 67877-230
Generic name: Mycophenolate mofetil
Labeler / Manufacturer: Ascend Laboratories, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SUSPENSION
Routes: ORAL
Marketing started: 20141117

FDA application: ANDA203005

## 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:"67877-230"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67877-230
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=21ff53b0-b4ba-4473-91e4-76ef41681064