United States · FDA National Drug Code directory
Mesalamine
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
- 63304-175_3f29d761-eab5-4f6b-a4f4-ffcc072648e3
- Product NDC
- 63304-175
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- Mesalamine
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190201
- Source listing expiry
- 20261231
Source-listed ingredients
- MESALAMINE — 1.2 g/1
These values do not establish equivalence or a dose recommendation.
Packages
- 120 TABLET, DELAYED RELEASE in 1 BOTTLE (63304-175-13) · 63304-175-13
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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