United States · FDA National Drug Code directory
DOXORUBICIN 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
- 68001-704_4dff7ee8-c0a2-c78d-e063-6394a90a79e8
- Product NDC
- 68001-704
- Form
- INJECTABLE, LIPOSOMAL
- Composition / generic term
- doxorubicin hydrochloride
- Labeler
- BluePoint Laboratories
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260402
- Source listing expiry
- 20271231
Source-listed ingredients
- DOXORUBICIN HYDROCHLORIDE — 2 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL, SINGLE-DOSE in 1 CARTON (68001-704-26) / 25 mL in 1 VIAL, SINGLE-DOSE · 68001-704-26
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 →