United States · FDA National Drug Code directory
Cefazolin
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
- 0409-2585_2d54e2f3-5269-4b4b-aac8-fc85b9d7a0b3
- Product NDC
- 0409-2585
- Form
- INJECTION, POWDER, FOR SOLUTION
- Composition / generic term
- Cefazolin
- Labeler
- Hospira, Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20070509 / 20260930
Source-listed ingredients
- CEFAZOLIN SODIUM — 1 g/1
These values do not establish equivalence or a dose recommendation.
Packages
- 25 VIAL in 1 CARTON (0409-2585-01) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0409-2585-11) · 0409-2585-01
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.
Browse United States records →