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
- 71288-158_598cecaa-f38c-451c-a3c8-55d90401b742
- Product NDC
- 71288-158
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Busulfan
- Labeler
- Meitheal Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20201023
- Source listing expiry
- 20261231
Source-listed ingredients
- BUSULFAN — 6 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 8 VIAL, SINGLE-DOSE in 1 CARTON (71288-158-96) / 10 mL in 1 VIAL, SINGLE-DOSE (71288-158-95) · 71288-158-96
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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