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
0069-0343_68af240b-3f2d-450c-b2bf-6f12d5176562
Product NDC
0069-0343
Form
INJECTION, SOLUTION
Composition / generic term
Doxorubicin Hydrochloride
Labeler
Pfizer Laboratories Div Pfizer Inc
Marketing category
NDA
Marketing start / end (source format)
20241111
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 (0069-0343-02) / 25 mL in 1 VIAL, SINGLE-DOSE · 0069-0343-02

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 →