Medicine
Cefuroxime 750 mg powder for injection
Cefuroxime 750 mg powder for injection is a generic prescription medicine for intramuscular, intravenous use, made by 2 labelers, with its source record on the US FDA register. It is available on request for export supply from India to licensed hospitals, importers and physicians.
Availability
Export supply from India to licensed buyers
Typical lead time
On request
Counted from payment and complete documents
Shipping
Ambient
Store at 20° to 25°C (68° to 77°F). Protect from light.
Key facts
- Active ingredient (INN)
- Cefuroxime
- Brand
- Sold under the generic name
- Strength
- 750 mg
- Dosage form
- Powder for injection
- Route
- Intramuscular, intravenous
- Packs
- 25 vials
- Manufacturers
- Hikma PharmaceuticalsSagent Pharmaceuticals
- Origin register
- US FDA, United States
- Storage
- Store at 20° to 25°C (68° to 77°F). Protect from light.
- Cold chain
- Not required on record
- Prescription status
- Prescription only
- Controlled substance
- Not recorded as controlled
- ATC code
- J01DC02 Cefuroxime
- HS code (indicative)
- 3004.20Indicative only. Your customs broker confirms the final tariff code.
- Marketing category
- marketed
- Marketed since
- 9 January 2004
- Identifiers
- RxCUI 1665444, 1665449DailyMed set ID 0a145288-733a-4966-b7ae-dc96eb103d8c, 703cc338-c0b6-4a02-b8db-c27aeff181df, 19902965-d2d6-433f-982d-0095014df4e8NDC 25021-118, 0143-9979, 0143-9568Application ANDA064125, ANDA065048
Record updated 12 November 2026
Documents available
Documents that can be provided with this medicine. Your regulator may ask for more, and the quote lists the full set.
No document list is recorded for this medicine yet. Tell us which documents your regulator needs (for example a CoA, COPP or GMP certificate) when you request a quote.
Packs
Packs from every labeler of this generic presentation.
| Pack | Code | Labeler | Marketed since |
|---|---|---|---|
| 25 vial in 1 carton / 1 injection, powder, for solution in 1 vial | 0143-9568-25 | Hikma Pharmaceuticals | 9 January 2004 |
| 25 vial in 1 carton / 1 injection, powder, for solution in 1 vial | 0143-9979-22 | Hikma Pharmaceuticals | 9 January 2004 |
| 25 vial in 1 carton / 1 injection, powder, for solution in 1 vial | 25021-118-10 | Sagent Pharmaceuticals | 1 September 2016 |
Status by register
Where this medicine is registered, from the source record and the regulator data we hold. Ask us about a country that is not listed.
| Register | Status | Source |
|---|---|---|
| US FDA | Listed, marketed | Source record for this pageChecked 12 November 2026 |
| US FDA | First approved 19 October 1983 | Drugs@FDA |
| EU (EMA) | Not recorded | — |
| India (CDSCO) | Not yet confirmed against CDSCO approval lists | — |
| United States | Registered | US FDA (NDC directory, openFDA)Checked 12 November 2026 |
Import route
Pick the destination country to see the legal import route, who applies and typical timelines, from our import guide for that country.
Import guides are available for 25 countries. Pick one to see its route summary.
BrazilColombiaEgyptEthiopiaGhanaIraqKazakhstanKenyaAll import guides
Other strengths and forms of Cefuroxime
Clinical summary
Cefuroxime is a cephalosporin antibacterial indicated for the treatment of patients with infections caused by susceptible strains of the designated organisms in diseases. MedsAcross supplies Cefuroxime for export from India to licensed hospitals, importers and physicians acting for named patients, with the documents each country requires.
Information from the US FDA prescribing information, retrieved 12 November 2026. Not yet medically reviewed.How we review
Read about CefuroximeFor healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.
Data sources
- DailyMed label record · Checked 12 November 2026
- Cefuroxime and Dextrose prescribing information (B. Braun Medical) · U.S. National Library of Medicine, DailyMed
Need Cefuroxime 750 mg powder for injection for your hospital or patient?
Send one request with the destination country and quantity. We confirm availability, lead time and the documents your regulator needs.