United States · FDA National Drug Code directory

Idarubicin Hydrochloride

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
0143-9218_894003f2-e5ea-430f-9450-aae8a493664e
Product NDC
0143-9218
Form
INJECTION, SOLUTION
Composition / generic term
Idarubicin Hydrochloride
Labeler
Hikma Pharmaceuticals USA Inc.
Marketing category
ANDA
Marketing start / end (source format)
20170130
Source listing expiry
20261231

Source-listed ingredients

  • IDARUBICIN HYDROCHLORIDE — 1 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 VIAL, GLASS in 1 BOX (0143-9218-01) / 10 mL in 1 VIAL, GLASS · 0143-9218-01

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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