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
0615-7768_4beb800d-fb92-42eb-a765-50ed0dfe1587
Product NDC
0615-7768
Form
TABLET, EXTENDED RELEASE
Composition / generic term
ISOSORBIDE MONONITRATE
Labeler
NCS HealthCare of KY, LLC dba Vangard Labs
Marketing category
ANDA
Marketing start / end (source format)
20110603
Source listing expiry
20261231

Source-listed ingredients

  • ISOSORBIDE MONONITRATE — 60 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 15 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-7768-05) · 0615-7768-05
  • 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-7768-39) · 0615-7768-39

Source and coverage

Open FDA National Drug Code directory

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.

Browse United States records →