# mycophenolate mofetil

NDC: 67877-266
Generic name: mycophenolate mofetil
Labeler / Manufacturer: Ascend Laboratories, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20100101

FDA application: ANDA200197

## Active ingredients

- MYCOPHENOLATE MOFETIL: 250 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"67877-266"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67877-266
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9f84ea84-2d8b-4d91-a33f-7dfb5df937dc