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
- 67877-225_f8b5a092-55fd-4e91-aa56-98fe69f1c091
- Product NDC
- 67877-225
- Form
- TABLET, FILM COATED
- Composition / generic term
- Mycophenolate Mofetil
- Labeler
- Ascend Laboratories, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20111128
- Source listing expiry
- 20271231
Source-listed ingredients
- MYCOPHENOLATE MOFETIL — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (67877-225-01) · 67877-225-01
- 500 TABLET, FILM COATED in 1 BOTTLE (67877-225-05) · 67877-225-05
- 10 BLISTER PACK in 1 CARTON (67877-225-38) / 10 TABLET, FILM COATED in 1 BLISTER PACK · 67877-225-38
- 3 BLISTER PACK in 1 CARTON (67877-225-84) / 10 TABLET, FILM COATED in 1 BLISTER PACK · 67877-225-84
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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