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
- 71610-033_11d3eb0d-489b-06c5-e063-6294a90a9d3b
- Product NDC
- 71610-033
- Form
- TABLET, FILM COATED
- Composition / generic term
- mycophenolate mofetil
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150106
- Source listing expiry
- 20261231
Source-listed ingredients
- MYCOPHENOLATE MOFETIL — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-033-53) · 71610-033-53
- 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-033-60) · 71610-033-60
- 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-033-70) · 71610-033-70
- 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-033-80) · 71610-033-80
- 240 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-033-90) · 71610-033-90
- 270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-033-92) · 71610-033-92
- 540 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-033-98) · 71610-033-98
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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