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
- 62756-827_d95f19dc-a686-42c7-88dc-997659b803df
- Product NDC
- 62756-827
- Form
- INJECTION, SOLUTION
- Composition / generic term
- DOXOrubicin Hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20120220
- Source listing expiry
- 20261231
Source-listed ingredients
- DOXORUBICIN HYDROCHLORIDE — 2 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL, MULTI-DOSE in 1 BOX (62756-827-40) / 100 mL in 1 VIAL, MULTI-DOSE · 62756-827-40
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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