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
- 72603-751_127eabe2-8386-452a-ad6b-d879e1f2c099
- Product NDC
- 72603-751
- Form
- POWDER, FOR SUSPENSION
- Composition / generic term
- mycophenolate mofetil
- Labeler
- NorthStar Rx LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260301
- Source listing expiry
- 20271231
Source-listed ingredients
- MYCOPHENOLATE MOFETIL — 200 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (72603-751-01) / 225 mL in 1 BOTTLE · 72603-751-01
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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