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
60219-1595_545a5c62-f746-4667-91ec-68673bfa787f
Product NDC
60219-1595
Form
POWDER, FOR SUSPENSION
Composition / generic term
Mycophenolate Mofetil
Labeler
Amneal Pharmaceuticals NY LLC
Marketing category
ANDA
Marketing start / end (source format)
20240321
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, PLASTIC in 1 CARTON (60219-1595-2) / 225 mL in 1 BOTTLE, PLASTIC · 60219-1595-2

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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