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Cefotaxime
CEP/COS
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Cefotaxime

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ACTIVE PHARMA INGREDIENTS

39 API Suppliers, 13 USDMF, 16 CEP/COS, 1 JDMF, 6 EU WC, 6 KDMF, 1 NDC API, 21 Listed Suppliers, $ API Reference Price

INTERMEDIATES

3 Intermediate Suppliers

3 Intermediate Suppliers

FINISHED DOSAGE FORMULATIONS

218 FDF Dossiers, 40 FDA Orange Book, 68 Europe, 2 Canada, 2 Australia, 27 South Africa, 79 Listed Dossiers

DRUG PRODUCT COMPOSITIONS

INJECTABLE;INJECTION - EQ 10GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, INJECTABLE;INJECTION - EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, INJECTABLE;INJECTION - EQ 2GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, INJECTABLE;INJECTION - EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

DIGITAL CONTENT

6 News #PharmaBuzz

6 News #PharmaBuzz

GLOBAL SALES INFORMATION

54 Regulatory FDF Prices

54 Regulatory FDF Prices

MARKET PLACE

20 APIs, 10 FDF Dossiers

REF. STANDARDS & IMPURITIES

3 EDQM, 2 USP, 2 Others

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Last Updated on PharmaCompass	Virtual Booth	Country	Certificate Holder	Certificate No.	Substance	Issue Date	Status	Type	End Date	Substance No.
28/03/2025	ACS DOBFAR SPA	Italy	ACS DOBFAR S.P.A. Tribiano IT	R1-CEP 1998-050 - Rev 03	Cefotaxime sodium, Sterile	2008-02-28	Valid	Chemical		989
28/03/2025	Aurobindo Pharma Limited	India	AUROBINDO PHARMA LIMITED Hyderabad IN	R1-CEP 2005-203 - Rev 01	Cefotaxime sodium, Sterile	2013-06-07	Withdrawn by Holder	Chemical	2014-02-06	989

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Cefotaxime

Cefotaxime

ACCESS ALL DATA

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CHEMISTRY

Discover Molecule Insights

ACTIVE PHARMA INGREDIENTS

39 API Suppliers

13 USDMF

16 CEP/COS

1 JDMF

6 EU WC

6 KDMF

1 NDC API

21 Listed Suppliers

$ API Reference Price

INTERMEDIATES

3 Intermediate Suppliers

FINISHED DOSAGE FORMULATIONS

218 FDF Dossiers

40 FDA Orange Book

68 Europe

2 Canada

2 Australia

27 South Africa

79 Listed Dossiers

DRUG PRODUCT COMPOSITIONS

INJECTABLE;INJECTION - EQ 10GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

INJECTABLE;INJECTION - EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

INJECTABLE;INJECTION - EQ 2GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

INJECTABLE;INJECTION - EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

DIGITAL CONTENT

6 News #PharmaBuzz

GLOBAL SALES INFORMATION

54 Regulatory FDF Prices

MARKET PLACE

20 APIs

10 FDF Dossiers

REF. STANDARDS & IMPURITIES

3 EDQM

2 USP

2 Others

Filters

INJECTABLE;INJECTION - EQ 10GM BASE/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons

INJECTABLE;INJECTION - EQ 1GM BASE/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons

INJECTABLE;INJECTION - EQ 2GM BASE/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons

INJECTABLE;INJECTION - EQ 500MG BASE/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons