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
68071-4290_1a3dc619-6b11-21b4-e063-6294a90acb1e
Product NDC
68071-4290
Form
TABLET, EXTENDED RELEASE
Composition / generic term
Isosorbide Mononitrate
Labeler
NuCare Pharmaceuticals,Inc.
Marketing category
ANDA
Marketing start / end (source format)
20170105
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 (68071-4290-3) · 68071-4290-3
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-4290-6) · 68071-4290-6
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-4290-9) · 68071-4290-9

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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