United States · FDA National Drug Code directory
Bortezomib
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
- 75007-501_1393b9d2-c8d3-49f9-8665-5cc3a083f0c7
- Product NDC
- 75007-501
- Form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Composition / generic term
- Bortezomib
- Labeler
- Ningbo Shuangcheng Pharmaceutical Co., Ltd.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20251217
- Source listing expiry
- 20261231
Source-listed ingredients
- BORTEZOMIB — 3.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL in 1 CARTON (75007-501-31) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL · 75007-501-31
- 1 VIAL in 1 CARTON (75007-501-32) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL · 75007-501-32
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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