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Cefalonium API Manufacturers & Suppliers

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Produced in  China
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Cefalonium | CAS No: 5575-21-3 | GMP-certified suppliers

A medication that provides antibacterial treatment for veterinary use, targeting bacterial infections caused by susceptible gram-positive and gram-negative organisms.

Therapeutic categories

Amidesbeta-LactamsHeterocyclic Compounds, Fused-RingLactamsSulfur CompoundsThiazines
Generic name
Cefalonium
Molecule type
small molecule
CAS number
5575-21-3
DrugBank ID
DB11385
Approval status
Experimental drug, Vet_approved drug

Product Snapshot

  • Cefalonium is a veterinary-approved injectable small molecule antibiotic
  • It is primarily used for treating bacterial infections in veterinary medicine
  • The product is currently experimental and approved for veterinary use but not authorized by human regulatory agencies such as FDA or EMA

Clinical Overview

Cefalonium, with CAS number 5575-21-3, is an experimental veterinary cephalosporin antibiotic. It belongs to the class of beta-lactam antibiotics characterized by a fused bicyclic ring system consisting of a 1,2-thiazine and a 2-azetidinone moiety. These structural features underpin its antibacterial activity typical of cephalosporins.

Cefalonium is primarily used in veterinary medicine, approved for use in certain animal treatments. Its clinical indications generally align with those of other cephalosporins, targeting bacterial infections caused by susceptible gram-positive and gram-negative organisms. Specific approved indications, dosing regimens, and species applications depend on regional regulatory approvals and veterinary clinical guidelines.

Pharmacologically, cefalonium disrupts bacterial cell wall synthesis by binding to penicillin-binding proteins (PBPs), inhibiting the cross-linking of peptidoglycan layers critical for cell wall integrity. This mechanism leads to bacterial cell lysis and death, characteristic of beta-lactam antibiotics.

Pharmacokinetic data, including absorption, distribution, metabolism, and excretion parameters, are limited for cefalonium. Generally, cephalosporins demonstrate variable oral bioavailability, with parenteral administration more common in veterinary settings. Elimination typically occurs via renal excretion, but specific ADME profiles for cefalonium require further elucidation.

Safety considerations for cefalonium involve potential hypersensitivity reactions common to beta-lactams, including anaphylaxis and allergic skin reactions. As with other cephalosporins, caution is advised in animals with known beta-lactam allergies. Toxicity data are primarily derived from veterinary studies, and human safety profiles are not established.

Cefalonium is marketed under various trade names within veterinary pharmaceutical portfolios. Its use is confined to animal health, with no approvals for human medical application.

For formulation scientists and procurement specialists, sourcing quality-assured cefalonium API requires compliance with veterinary pharmaceutical standards and verification of batch consistency. Given its experimental and veterinary-approved status, manufacturers should ensure adherence to Good Manufacturing Practices (GMP) and regulatory requirements pertinent to animal health products. Certificates of analysis and impurity profiles must be thoroughly reviewed during API procurement to maintain product safety and efficacy.

Identification & chemistry

Generic name Cefalonium
Molecule type Small molecule
CAS 5575-21-3
UNII K2P920217W
DrugBank ID DB11385

Formulation & handling

  • Cefalonium is a small molecule cephalosporin primarily used in veterinary applications, typically formulated for injectable administration.
  • Its low logP and poor water solubility require consideration for solubilization strategies during formulation.
  • Stability may be sensitive to hydrolysis, necessitating controlled storage conditions to maintain API integrity.

Regulatory status

Cefalonium is a type of Other substances


The pharmaceutical industry encompasses a diverse range of active pharmaceutical ingredients (APIs) that are used in the production of various medications. One category of APIs is known as other substances. This category includes substances that do not fall under the conventional classifications such as antibiotics, analgesics, or antihypertensives.

Other substances in pharmaceutical APIs consist of a broad array of chemical compounds with unique properties and applications. These substances play a crucial role in the formulation and development of specialized medications, catering to specific therapeutic needs. The category encompasses various substances like excipients, solvents, stabilizers, and pH adjusters.

Excipients are inert substances that aid in the manufacturing process and enhance the stability, bioavailability, and patient acceptability of pharmaceutical formulations. Solvents are used to dissolve other ingredients and facilitate their incorporation into the final product. Stabilizers ensure the integrity and shelf life of medications by preventing degradation or chemical changes. pH adjusters help maintain the desired pH level of a formulation, which can influence the drug's efficacy and stability.

Pharmaceutical manufacturers carefully select and incorporate specific other substances into their formulations, adhering to regulatory guidelines and quality standards. These substances undergo rigorous testing and evaluation to ensure their safety, efficacy, and compatibility with the desired pharmaceutical product. By employing other substances in API formulations, pharmaceutical companies can optimize drug delivery, improve patient compliance, and enhance therapeutic outcomes.

In summary, the other substances category of pharmaceutical APIs comprises a diverse range of chemicals, including excipients, solvents, stabilizers, and pH adjusters. These substances contribute to the formulation, stability, and performance of medications, enabling pharmaceutical manufacturers to develop specialized products that meet specific therapeutic requirements.

Cefalonium API manufacturers & distributors

Compare qualified Cefalonium API suppliers worldwide. We currently have 1 companies offering Cefalonium API, with manufacturing taking place in 1 different countries. Use the table below to review supplier type, countries of origin, certifications, product portfolio and GMP audit availability.

SupplierTypeCountryProduct originCertificationsPortfolio
Producer
China China BSE/TSE, CoA, EDMF/ASMF, GMP, ISO14001, ISO9001, MSDS, USDMF235 products

When sending a request, specify which Cefalonium API quality you need: for example EP (Ph. Eur.), USP, JP, BP, or another pharmacopoeial standard, as well as the required grade (base, salt, micronised, specific purity, etc.).

Use the list above to find high-quality Cefalonium API suppliers. For example, you can select GMP, FDA or ISO certified suppliers. Visit our help page to learn more about sourcing APIs via Pharmaoffer.