United States · FDA National Drug Code directory
Daunorubicin 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
- 42658-019_48b4337a-9cc5-665d-e063-6294a90a1613
- Product NDC
- 42658-019
- Form
- INJECTION, SOLUTION
- Composition / generic term
- daunorubicin hydrochloride
- Labeler
- Hisun Pharmaceuticals USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200120
- Source listing expiry
- 20271231
Source-listed ingredients
- DAUNORUBICIN HYDROCHLORIDE — 5 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL in 1 BOX (42658-019-01) / 10 mL in 1 VIAL · 42658-019-01
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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