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
72485-415_42edff88-f01d-0908-e063-6294a90a3b0f
Product NDC
72485-415
Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Composition / generic term
mycophenolate mofetil
Labeler
ARMAS PHARMACEUTICALS INC
Marketing category
ANDA
Marketing start / end (source format)
20230706
Source listing expiry
20261231

Source-listed ingredients

  • MYCOPHENOLATE MOFETIL — 500 mg/20mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 4 VIAL in 1 CARTON (72485-415-04) / 20 mL in 1 VIAL · 72485-415-04

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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