United States · FDA National Drug Code directory

MYCOPHENOLATE MOFETIL

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 59651-646_83531645-459d-4746-bc46-2d32928e9417
Product NDC: 59651-646
Form: POWDER, FOR SUSPENSION
Composition / generic term: mycophenolate mofetil
Labeler: Aurobindo Pharma Limited
Marketing category: ANDA
Marketing start / end (source format): 20240926
Source listing expiry: 20261231

Source-listed ingredients

MYCOPHENOLATE MOFETIL — 200 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

1 BOTTLE in 1 CARTON (59651-646-26) / 225 mL in 1 BOTTLE · 59651-646-26

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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