United States · FDA National Drug Code directory
CYCLOPHOSPHAMIDE
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
- 83703-549_450da59c-b50e-4de0-e063-6394a90a0559
- Product NDC
- 83703-549
- Form
- INJECTION, POWDER, FOR SOLUTION
- Composition / generic term
- cyclophosphamide
- Labeler
- Bamboo US Bidco LCC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20080521
- Source listing expiry
- 20261231
Source-listed ingredients
- CYCLOPHOSPHAMIDE — 500 mg/25mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL, SINGLE-DOSE in 1 CARTON (83703-549-01) / 25 mL in 1 VIAL, SINGLE-DOSE (83703-549-25) · 83703-549-01
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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