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
- 0781-2067_8d255117-cfa8-4893-8e2e-945eee7b12c4
- Product NDC
- 0781-2067
- Form
- CAPSULE
- Composition / generic term
- Mycophenolate Mofetil
- Labeler
- Sandoz Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20081015
- Source listing expiry
- 20261231
Source-listed ingredients
- MYCOPHENOLATE MOFETIL — 250 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE in 1 BOTTLE (0781-2067-01) · 0781-2067-01
- 500 CAPSULE in 1 BOTTLE (0781-2067-05) · 0781-2067-05
- 120 CAPSULE in 1 BOTTLE (0781-2067-72) · 0781-2067-72
- 12 CAPSULE in 1 CARTON (0781-2067-89) · 0781-2067-89
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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