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
- 23155-848_b5316b1d-ed7b-426d-9b86-dd17018c97a5
- Product NDC
- 23155-848
- Form
- POWDER, FOR SUSPENSION
- Composition / generic term
- MYCOPHENOLATE MOFETIL
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230905 / 20280229
Source-listed ingredients
- MYCOPHENOLATE MOFETIL — 200 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, PLASTIC in 1 CARTON (23155-848-51) / 225 mL in 1 BOTTLE, PLASTIC · 23155-848-51
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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