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
- 68254-5003_6eb2ddd0-ab23-44ae-a1ce-acc44e4f7e29
- Product NDC
- 68254-5003
- Form
- TABLET
- Composition / generic term
- MYCOPHENOLATE MOFETIL
- Labeler
- CONCORD BIOTECH LIMITED
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20201221
- Source listing expiry
- 20261231
Source-listed ingredients
- MYCOPHENOLATE MOFETIL — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (68254-5003-1) · 68254-5003-1
- 100 TABLET in 1 BOTTLE (68254-5003-2) · 68254-5003-2
- 500 TABLET in 1 BOTTLE (68254-5003-3) · 68254-5003-3
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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