United States · FDA National Drug Code directory

Busulfan

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
51817-170_df501797-3c7e-5ae2-e053-2995a90a99e8
Product NDC
51817-170
Form
INJECTION
Composition / generic term
busulfan
Labeler
Pharmascience Inc.
Marketing category
ANDA
Marketing start / end (source format)
20170519
Source listing expiry
20261231

Source-listed ingredients

  • BUSULFAN — 6 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 8 VIAL in 1 PACKAGE (51817-170-01) / 10 mL in 1 VIAL · 51817-170-01

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.

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