United States · FDA National Drug Code directory
Cefuroxime
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
- 0143-9976_5621cde0-74c5-45b2-8f76-329eb22b4a0a
- Product NDC
- 0143-9976
- Form
- INJECTION, POWDER, FOR SOLUTION
- Composition / generic term
- Cefuroxime
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20040109
- Source listing expiry
- 20261231
Source-listed ingredients
- CEFUROXIME SODIUM — 750 mg/8mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (0143-9976-03) / 82.5 mL in 1 VIAL, PHARMACY BULK PACKAGE (0143-9976-91) · 0143-9976-03
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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