Cefuroxime Axetil

PharmaCompass offers a list of Cefuroxime Axetil API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Cefuroxime Axetil manufacturer or Cefuroxime Axetil supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cefuroxime Axetil manufacturer or Cefuroxime Axetil supplier.

PharmaCompass also assists you with knowing the Cefuroxime Axetil API Price utilized in the formulation of products. Cefuroxime Axetil API Price is not always fixed or binding as the Cefuroxime Axetil Price is obtained through a variety of data sources. The Cefuroxime Axetil Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Cefuroxime Axetil

Synonyms

97232-96-7, Cefuroxime axetil, (e)-, 64544-07-6, (+/-)-cefuroxime axetil, (e)-, Xsl6i3sb26, Ceftin

Cas Number

64544-07-6

Unique Ingredient Identifier (UNII)

XSL6I3SB26

About Cefuroxime Axetil

Cefuroxime Axetil is a second generation semi-synthetic cephalosporin and a beta-lactam antibiotic with bactericidal activity. Cefuroxime's effect is dependent on its binding to penicillin-binding proteins (PBPs) located in the bacterial cytoplasmic membrane. Binding results in the inhibition of the transpeptidase enzymes, thereby preventing cross-linking of the pentaglycine bridge with the fourth residue of the pentapeptide and interrupting consequent synthesis of peptidoglycan chains. As a result, cefuroxime inhibits bacterial septum and cell wall synthesis formation.

Cefuroxime Axetil Manufacturers

A Cefuroxime Axetil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cefuroxime Axetil, including repackagers and relabelers. The FDA regulates Cefuroxime Axetil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cefuroxime Axetil API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

click here to find a list of Cefuroxime Axetil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Cefuroxime Axetil Suppliers

A Cefuroxime Axetil supplier is an individual or a company that provides Cefuroxime Axetil active pharmaceutical ingredient (API) or Cefuroxime Axetil finished formulations upon request. The Cefuroxime Axetil suppliers may include Cefuroxime Axetil API manufacturers, exporters, distributors and traders.

click here to find a list of Cefuroxime Axetil suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Cefuroxime Axetil KDMF

In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.

Pharmaceutical companies submit a Cefuroxime Axetil Drug Master File in Korea (Cefuroxime Axetil KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Cefuroxime Axetil. The MFDS reviews the Cefuroxime Axetil KDMF as part of the drug registration process and uses the information provided in the Cefuroxime Axetil KDMF to evaluate the safety and efficacy of the drug.

After submitting a Cefuroxime Axetil KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Cefuroxime Axetil API can apply through the Korea Drug Master File (KDMF).

click here to find a list of Cefuroxime Axetil suppliers with KDMF on PharmaCompass.

Cefuroxime Axetil Manufacturers | Traders | Suppliers

We have 8 companies offering Cefuroxime Axetil

Get in contact with the supplier of your choice:

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.

List of Drug Master Files (KDMF) for Cefuroxime Axetil Active Pharmaceutical Ingredient (API) submitted to the Review Authority in Korea.

Cefuroxime Axetil

Synopsis

Chemistry

APIs // Active Pharmaceutical Ingredients

59 Suppliers

40 USDMF

20 CEP/COS

11 EU WC

24 KDMF

4 NDC API

16 Listed Suppliers

DEVELOPMENTS

2 Drug(s) in Development

PRICE INFORMATION

API Reference Price

API Exports

API Imports

FDF Exports

FDF Imports

INTERMEDIATES

1 Suppliers

DOSSIERs // Finished Dosage Forms

216 Dossiers

34 FDA Orange Book

113 Europe

5 Canada

8 South Africa

56 Listed Dossiers

DRUG PRODUCT COMPOSITION

TABLET;ORAL - EQ 125MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

TABLET;ORAL - EQ 250MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

TABLET;ORAL - EQ 500MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

FOR SUSPENSION;ORAL - EQ 125MG BASE/5ML

FOR SUSPENSION;ORAL - EQ 250MG BASE/5ML

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Suppliers

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1 Evonik

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TABLET;ORAL - EQ 125MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons

TABLET;ORAL - EQ 250MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons

TABLET;ORAL - EQ 500MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons