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
- 54288-141_1a8abd3a-6834-4468-a443-ca95e795b17d
- Product NDC
- 54288-141
- Form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Composition / generic term
- Mycophenolate Mofetil hydrochloride
- Labeler
- BPI Labs LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230308
- Source listing expiry
- 20261231
Source-listed ingredients
- MYCOPHENOLATE MOFETIL HYDROCHLORIDE — 500 mg/20mL
These values do not establish equivalence or a dose recommendation.
Packages
- 4 VIAL in 1 CARTON (54288-141-04) / 20 mL in 1 VIAL · 54288-141-04
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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