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Cefuroxime Sodium

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ACTIVE PHARMA INGREDIENTS

31 API Suppliers, 13 USDMF, 14 CEP/COS, 4 EU WC, 1 KDMF, 1 NDC API, 12 Listed Suppliers, $ API Reference Price

FINISHED DOSAGE FORMULATIONS

224 FDF Dossiers, 35 FDA Orange Book, 79 Europe, 2 Canada, 8 Australia, 52 South Africa, 48 Listed Dossiers

DRUG PRODUCT COMPOSITIONS

INJECTABLE;INJECTION - EQ 1.5GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, INJECTABLE;INJECTION - EQ 7.5GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, INJECTABLE;INTRAMUSCULAR, INTRAVENOUS - EQ 750MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, INJECTABLE;INJECTION - EQ 30MG BASE/ML

RELATED EXCIPIENT COMPANIES

2 Kirsch Pharma, 1 Actylis, 1 Kerry, 1 Microlex e.U, 1 Pluviaendo, 1 Roquette

EXCIPIENTS BY APPLICATIONS

4 Parenteral, 2 Fillers, Diluents & Binders, 1 Chewable & Orodispersible Aids, 1 Taste Masking

DIGITAL CONTENT

1 News #PharmaBuzz

1 News #PharmaBuzz

GLOBAL SALES INFORMATION

2 US Medicaid Prescriptions, 22 Regulatory FDF Prices

MARKET PLACE

12 APIs, 5 FDF Dossiers

REF. STANDARDS & IMPURITIES

1 EDQM, 1 Others

ANALYTICAL

1 BioAnalytical Methods

1 BioAnalytical Methods

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Last Updated on PharmaCompass	Virtual Booth	Country	Registrant Name	Registration No.	Compound	Registration Date	Manufacturer	Manufacturer's Country	Manufacturer's Address
31/10/2025	Kyongbo Pharmaceutical Co., Ltd	South Korea	Kyungbo Pharmaceutical Co., Ltd.	20190102-210-J-292	cefuroxime sodium	2019-01-02	Kyungbo Pharmaceutical Co., Ltd. @ [Starting Material: Cefuroxime Manufacturing Plant] Sinopharm Weiqida Pharmaceutical Co., Ltd	South Korea	174 Silok-ro, Asan-si, Chungcheongnam-do @ [Starting material: Cefuroxime manufacturing plant] Economic & Technological Development Zone, First Medical Zone, Datong, Shanxi China

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Cefuroxime Sodium

Cefuroxime Sodium

ACCESS ALL DATA

Browse all information

CHEMISTRY

Discover Molecule Insights

ACTIVE PHARMA INGREDIENTS

31 API Suppliers

13 USDMF

14 CEP/COS

4 EU WC

1 KDMF

1 NDC API

12 Listed Suppliers

$ API Reference Price

FINISHED DOSAGE FORMULATIONS

224 FDF Dossiers

35 FDA Orange Book

79 Europe

2 Canada

8 Australia

52 South Africa

48 Listed Dossiers

DRUG PRODUCT COMPOSITIONS

INJECTABLE;INJECTION - EQ 1.5GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

INJECTABLE;INJECTION - EQ 7.5GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

INJECTABLE;INTRAMUSCULAR, INTRAVENOUS - EQ 750MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

INJECTABLE;INJECTION - EQ 30MG BASE/ML

RELATED EXCIPIENT COMPANIES

2 Kirsch Pharma

1 Actylis

1 Kerry

1 Microlex e.U

1 Pluviaendo

1 Roquette

EXCIPIENTS BY APPLICATIONS

4 Parenteral

2 Fillers, Diluents & Binders

1 Chewable & Orodispersible Aids

1 Taste Masking

DIGITAL CONTENT

1 News #PharmaBuzz

GLOBAL SALES INFORMATION

2 US Medicaid Prescriptions

22 Regulatory FDF Prices

MARKET PLACE

12 APIs

5 FDF Dossiers

REF. STANDARDS & IMPURITIES

1 EDQM

1 Others

ANALYTICAL

1 BioAnalytical Methods

Filters

INJECTABLE;INJECTION - EQ 1.5GM BASE/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons

INJECTABLE;INJECTION - EQ 7.5GM BASE/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons

INJECTABLE;INTRAMUSCULAR, INTRAVENOUS - EQ 750MG BASE/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons