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
- 67877-426_27fbf61b-de1e-479a-9d04-6dc1d48f3148
- Product NDC
- 67877-426
- 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 — 180 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 500 TABLET, DELAYED RELEASE in 1 BOTTLE (67877-426-05) · 67877-426-05
- 120 TABLET, DELAYED RELEASE in 1 BOTTLE (67877-426-12) · 67877-426-12
- 10 BLISTER PACK in 1 CARTON (67877-426-38) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (67877-426-33) · 67877-426-38
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →