# MYCOPHENOLATE MOFETIL

NDC: 64380-899
Generic name: MYCOPHENOLATE MOFETIL
Labeler / Manufacturer: Strides Pharma Science Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SUSPENSION
Routes: ORAL
Marketing started: 20260901

FDA application: ANDA212634

## 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:"64380-899"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=64380-899
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c1c4cb31-00a7-417e-9775-24e849d62791