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Looking for 61622-34-2 / Cefotiam API manufacturers, exporters & distributors?

Cefotiam manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Cefotiam

Synonyms

61622-34-2, Cefotiamum, Cefotiamum [inn-latin], Ceradon, Aspil, Ctm

Cas Number

61622-34-2

Unique Ingredient Identifier (UNII)

91W6Z2N718

About Cefotiam

One of the CEPHALOSPORINS that has a broad spectrum of activity against both gram-positive and gram-negative microorganisms.

Cefotiam Manufacturers

A Cefotiam manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cefotiam, including repackagers and relabelers. The FDA regulates Cefotiam manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cefotiam 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 Cefotiam manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Cefotiam Suppliers

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

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

Cefotiam USDMF

A Cefotiam DMF (Drug Master File) is a document detailing the whole manufacturing process of Cefotiam active pharmaceutical ingredient (API) in detail. Different forms of Cefotiam DMFs exist exist since differing nations have different regulations, such as Cefotiam USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A Cefotiam DMF submitted to regulatory agencies in the US is known as a USDMF. Cefotiam USDMF includes data on Cefotiam's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Cefotiam USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of Cefotiam suppliers with USDMF on PharmaCompass.

Cefotiam GMP

Cefotiam 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 Cefotiam 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 Cefotiam GMP manufacturer or Cefotiam GMP API supplier for your needs.

Cefotiam CoA

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

Cefotiam CoA mostly includes findings from lab analyses of a specific batch. For each Cefotiam 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.

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