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
- 67457-386_4c643876-2577-4197-ac9b-81bab65d1362
- Product NDC
- 67457-386
- Form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Composition / generic term
- Mycophenolate Mofetil
- Labeler
- Mylan Institutional LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210126
- 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 (67457-386-81) / 20 mL in 1 VIAL (67457-386-00) · 67457-386-81
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →