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
59651-540_55810c9d-1140-40b8-a297-210a84afc05a
Product NDC
59651-540
Form
TABLET, EXTENDED RELEASE
Composition / generic term
ISOSORBIDE MONONITRATE
Labeler
Aurobindo Pharma Limited
Marketing category
ANDA
Marketing start / end (source format)
20221107
Source listing expiry
20261231

Source-listed ingredients

  • ISOSORBIDE MONONITRATE — 60 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-540-01) · 59651-540-01
  • 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-540-05) · 59651-540-05

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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