United States · FDA National Drug Code directory

MYCOPHENOLIC ACID

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
67877-427_27fbf61b-de1e-479a-9d04-6dc1d48f3148
Product NDC
67877-427
Form
TABLET, DELAYED RELEASE
Composition / generic term
MYCOPHENOLIC ACID
Labeler
Ascend Laboratories, LLC
Marketing category
ANDA
Marketing start / end (source format)
20210924
Source listing expiry
20271231

Source-listed ingredients

  • MYCOPHENOLATE SODIUM — 360 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 500 TABLET, DELAYED RELEASE in 1 BOTTLE (67877-427-05) · 67877-427-05
  • 120 TABLET, DELAYED RELEASE in 1 BOTTLE (67877-427-12) · 67877-427-12
  • 10 BLISTER PACK in 1 CARTON (67877-427-38) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (67877-427-33) · 67877-427-38

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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