# mycophenolate mofetil

NDC: 16729-019
Generic name: mycophenolate mofetil
Labeler / Manufacturer: Accord Healthcare Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20090504

FDA application: ANDA065416

## Active ingredients

- MYCOPHENOLATE MOFETIL: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"16729-019"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16729-019
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=741e079a-646b-47ec-84ac-8e12574c2aaf