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
42677-307_47b286d2-bbaf-75ff-e063-6294a90a6de7
Product NDC
42677-307
Form
TABLET, EXTENDED RELEASE
Composition / generic term
Isosorbide Mononitrate
Labeler
Shandong New Time Pharmaceutical Co., Ltd.
Marketing category
ANDA
Marketing start / end (source format)
20220429
Source listing expiry
20271231

Source-listed ingredients

  • ISOSORBIDE MONONITRATE — 120 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (42677-307-01) · 42677-307-01
  • 600 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (42677-307-02) · 42677-307-02

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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