United States · FDA National Drug Code directory
Ceftriaxone Sodium
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
- 60505-6152_0432e6c3-ad77-726c-e063-6294a90a798c
- Product NDC
- 60505-6152
- Form
- INJECTION, POWDER, FOR SOLUTION
- Composition / generic term
- Ceftriaxone Sodium
- Labeler
- Apotex Corp.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170630
- Source listing expiry
- 20261231
Source-listed ingredients
- CEFTRIAXONE SODIUM — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL, SINGLE-USE in 1 CARTON (60505-6152-1) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE · 60505-6152-1
- 1 VIAL, SINGLE-USE in 1 CARTON (60505-6152-4) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE · 60505-6152-4
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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