United States · FDA National Drug Code directory

Isosorbide Mononitrate

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
71610-788_ed4b9b65-54be-40f0-b2d0-452b7d1b49c4
Product NDC
71610-788
Form
TABLET, EXTENDED RELEASE
Composition / generic term
Isosorbide Mononitrate
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Marketing category
ANDA
Marketing start / end (source format)
20181105
Source listing expiry
20261231

Source-listed ingredients

  • ISOSORBIDE MONONITRATE — 30 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71610-788-30) · 71610-788-30
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71610-788-60) · 71610-788-60

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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