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
70710-1302_466a93ff-b90a-4e04-b440-8b26e3f95c63
Product NDC
70710-1302
Form
SUPPOSITORY
Composition / generic term
Mesalamine
Labeler
Zydus Pharmaceuticals USA Inc.
Marketing category
ANDA
Marketing start / end (source format)
20200214
Source listing expiry
20261231

Source-listed ingredients

  • MESALAMINE — 1000 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 5 BLISTER PACK in 1 POUCH (70710-1302-7) / 6 SUPPOSITORY in 1 BLISTER PACK (70710-1302-6) · 70710-1302-7

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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