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01 4CKD BIO CORPORATION Ansan-si KR

02 3DEVA HOLDING A.Ş. Istanbul TR

03 2FERMIC, S.A. DE C.V. Mexico City MX

04 2Fermic SA de CV Iztapalapa MX

05 7LEK PHARMACEUTICALS D.D. Ljubljana SI

06 1SANDOZ INDUSTRIAL PRODUCTS S.A. Palafolls ES

07 3SHANDONG NEW TIME PHARMACEUTICAL CO., LTD. Linyi CN

08 2SINOPHARM WEIQIDA PHARMACEUTICAL CO., LTD Datong CN

09 1SMITHKLINE BEECHAM LIMITED Irvine GB

10 1Sandoz Industrial Products SpA Rovereto IT

11 2Smithkline Beecham Pharmaceuticals Irvine GB

12 1Smithkline Beecham Pharmaceuticals Worthing GB

13 4ZHUHAI UNITED LABORATORIES CO., LTD. Sanzao Town CN

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PharmaCompass

Looking for 61177-45-5 / Clavulanic Acid API manufacturers, exporters & distributors?

Clavulanic Acid manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Clavulanic Acid

Synonyms

Potassium clavulanate, 61177-45-5, Clavulanic acid potassium salt, Brl 14151k, Clavulanate (potassium), Q42omw3at8

Cas Number

61177-45-5

Unique Ingredient Identifier (UNII)

Q42OMW3AT8

About Clavulanic Acid

A beta-lactam antibiotic produced by the actinobacterium Streptomyces clavuligerus. It is a suicide inhibitor of bacterial beta-lactamase enzymes. Administered alone, it has only weak antibacterial activity against most organisms, but given in combination with other beta-lactam antibiotics it prevents antibiotic inactivation by microbial lactamase.

AUGMENTIN XR-1 Manufacturers

A AUGMENTIN XR-1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AUGMENTIN XR-1, including repackagers and relabelers. The FDA regulates AUGMENTIN XR-1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AUGMENTIN XR-1 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 AUGMENTIN XR-1 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

AUGMENTIN XR-1 Suppliers

A AUGMENTIN XR-1 supplier is an individual or a company that provides AUGMENTIN XR-1 active pharmaceutical ingredient (API) or AUGMENTIN XR-1 finished formulations upon request. The AUGMENTIN XR-1 suppliers may include AUGMENTIN XR-1 API manufacturers, exporters, distributors and traders.

click here to find a list of AUGMENTIN XR-1 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

AUGMENTIN XR-1 CEP

A AUGMENTIN XR-1 CEP of the European Pharmacopoeia monograph is often referred to as a AUGMENTIN XR-1 Certificate of Suitability (COS). The purpose of a AUGMENTIN XR-1 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of AUGMENTIN XR-1 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of AUGMENTIN XR-1 to their clients by showing that a AUGMENTIN XR-1 CEP has been issued for it. The manufacturer submits a AUGMENTIN XR-1 CEP (COS) as part of the market authorization procedure, and it takes on the role of a AUGMENTIN XR-1 CEP holder for the record. Additionally, the data presented in the AUGMENTIN XR-1 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the AUGMENTIN XR-1 DMF.

A AUGMENTIN XR-1 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. AUGMENTIN XR-1 CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.

click here to find a list of AUGMENTIN XR-1 suppliers with CEP (COS) on PharmaCompass.

AUGMENTIN XR-1 Manufacturers | Traders | Suppliers

AUGMENTIN XR-1 Manufacturers, Traders, Suppliers 1
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.