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  • FOR SUSPENSION;ORAL - EQ 180MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • FOR SUSPENSION;ORAL - EQ 90MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Looking for 118081-34-8 / Ceftibuten Dihydrate API manufacturers, exporters & distributors?

Ceftibuten Dihydrate manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Ceftibuten Dihydrate 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 Ceftibuten Dihydrate manufacturer or Ceftibuten Dihydrate supplier for your needs.

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

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

API | Excipient name

Ceftibuten Dihydrate

Synonyms

118081-34-8, Ceftibuten (dihydrate), Ceftibuten.2h2o, Isocef, 62f4443rwp, Ceftibuten hydrate

Cas Number

118081-34-8

Unique Ingredient Identifier (UNII)

62F4443RWP

About Ceftibuten Dihydrate

Ceftibuten Dihydrate is the dihydrate form of ceftibuten, a semisynthetic, beta-lactamase-stable, third-generation cephalosporin with antibacterial activity. Ceftibuten binds to and inactivates penicillin-binding proteins (PBPs) located on the inner membrane of the bacterial cell wall. PBPs are enzymes involved in the terminal stages of assembling the bacterial cell wall and in reshaping the cell wall during growth and division. Inactivation of PBPs interferes with the cross-linkage of peptidoglycan chains necessary for bacterial cell wall strength and rigidity. This results in the weakening of the bacterial cell wall and causes cell lysis.

Ceftibuten Dihydrate Manufacturers

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

Ceftibuten Dihydrate Suppliers

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

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

Ceftibuten Dihydrate WC

A Ceftibuten Dihydrate written confirmation (Ceftibuten Dihydrate WC) is an official document issued by a regulatory agency to a Ceftibuten Dihydrate manufacturer, verifying that the manufacturing facility of a Ceftibuten Dihydrate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Ceftibuten Dihydrate APIs or Ceftibuten Dihydrate finished pharmaceutical products to another nation, regulatory agencies frequently require a Ceftibuten Dihydrate WC (written confirmation) as part of the regulatory process.

click here to find a list of Ceftibuten Dihydrate suppliers with Written Confirmation (WC) on PharmaCompass.

Ceftibuten Dihydrate GMP

Ceftibuten Dihydrate Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.

GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).

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

Ceftibuten Dihydrate CoA

A Ceftibuten Dihydrate CoA (Certificate of Analysis) is a formal document that attests to Ceftibuten Dihydrate's compliance with Ceftibuten Dihydrate specifications and serves as a tool for batch-level quality control.

Ceftibuten Dihydrate CoA mostly includes findings from lab analyses of a specific batch. For each Ceftibuten Dihydrate CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.

Ceftibuten Dihydrate may be tested according to a variety of international standards, such as European Pharmacopoeia (Ceftibuten Dihydrate EP), Ceftibuten Dihydrate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Ceftibuten Dihydrate USP).

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.
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