01 3CIPAN - COMPANHIA INDUSTRIAL PRODUTORA DE ANTIBIOTICOS, S.A. Castanheira Do Ribatejo PT
02 4CKD BIO CORPORATION Ansan-si KR
03 3DEVA HOLDING A.Ş. Istanbul TR
04 3DSM Anti-Infectives B.V. Delft NL
05 2FERMIC, S.A. DE C.V. Mexico City MX
06 2Fermic SA de CV Iztapalapa MX
07 7LEK PHARMACEUTICALS D.D. Ljubljana SI
08 1SANDOZ INDUSTRIAL PRODUCTS S.A. Palafolls ES
09 3SHANDONG NEW TIME PHARMACEUTICAL CO., LTD. Linyi CN
10 3SINOPHARM WEIQIDA PHARMACEUTICAL CO., LTD Datong CN
11 1SMITHKLINE BEECHAM LIMITED Irvine GB
12 1Sandoz Industrial Products SpA Rovereto IT
13 2Smithkline Beecham Pharmaceuticals Irvine GB
14 1Smithkline Beecham Pharmaceuticals Worthing GB
15 4ZHUHAI UNITED LABORATORIES CO., LTD. Sanzao Town CN
01 10Potassium clavulanate
02 1Potassium clavulanate, Code Number 472803
03 3Potassium clavulanate, Sterile
04 1Potassium clavulanate, diluted, Microcrystalline cellulose 1:1 blend
05 2Potassium clavulanate, diluted, With microcrystalline cellulose in the ratio 1:1
06 1Potassium clavulanate, diluted, With silica, colloidal hydrated in the ratio 1:1
07 1Potassium clavulanate, diluted, With silicone dioxide in the ratio 1:1
08 1Potassium clavulanate, diluted, silica, colloidal hydrated in a ratio 1:1
09 1Potassium clavulanate, diluted, with cellulose microcrystalline (0316) in ratio 1:1
10 1Potassium clavulanate, diluted, with microcrystalline Cellulose in the ratio 7:3
11 1Potassium clavulanate, diluted, with microcrystalline cellulose in a ratio 1:1
12 1Potassium clavulanate, diluted, with microcrystalline cellulose in a ratio of 1:1
13 1Potassium clavulanate, diluted, with microcrystalline cellulose in a ratio of 3:2
14 5Potassium clavulanate, diluted, with microcrystalline cellulose in the ratio 1:1
15 2Potassium clavulanate, diluted, with microcrystalline cellulose in the ratio 7:3
16 1Potassium clavulanate, diluted, with silica, colloidal anhydrous (0434) in ratio 1:1
17 1Potassium clavulanate, diluted, with silica, colloidal anhydrous in a ratio of 1:1
18 1Potassium clavulanate, diluted, with silica, colloidal hydrated in a ratio of 1:1
19 3Potassium clavulanate, diluted, with silica, colloidal hydrated in the ratio 1:1
20 2Potassium clavulanate, diluted, with silicon dioxide in the ratio 1:1
01 10China
02 1Germany
03 1Italy
04 4Mexico
05 3Netherlands
06 3Portugal
07 7Slovenia
08 4South Korea
09 3Turkey
10 4United Kingdom
01 4Expired
02 29Valid
03 7Withdrawn by Holder
Potassium Clavulanate, Sterile
Certificate Number : R1-CEP 1999-113 - Rev 04
Status : Valid
Issue Date : 2014-02-26
Type : Chemical
Substance Number : 1140
Potassium Clavulanate, Diluted, With Microcrysta...
Certificate Number : R1-CEP 2007-258 - Rev 02
Status : Valid
Issue Date : 2021-03-05
Type : Chemical
Substance Number : 1653
Potassium Clavulanate, Diluted, With Microcrysta...
Certificate Number : R1-CEP 2007-259 - Rev 02
Status : Valid
Issue Date : 2021-03-05
Type : Chemical
Substance Number : 1653
Potassium Clavulanate, Diluted, With Silica, Col...
Certificate Number : R1-CEP 2007-260 - Rev 02
Status : Valid
Issue Date : 2021-03-08
Type : Chemical
Substance Number : 1653
Potassium Clavulanate, Diluted, With Silica, Col...
Certificate Number : R1-CEP 2004-241 - Rev 03
Status : Valid
Issue Date : 2020-02-07
Type : Chemical
Substance Number : 1653
Potassium Clavulanate, Diluted, With Microcrysta...
Certificate Number : R1-CEP 2004-242 - Rev 03
Status : Valid
Issue Date : 2020-02-07
Type : Chemical
Substance Number : 1653
Potassium Clavulanate, Code Number 472803
Certificate Number : R1-CEP 1998-001 - Rev 09
Status : Valid
Issue Date : 2020-02-25
Type : Chemical
Substance Number : 1140
Certificate Number : R1-CEP 2014-320 - Rev 00
Status : Valid
Issue Date : 2021-03-05
Type : Chemical
Substance Number : 1140
Potassium Clavulanate, Diluted, With Cellulose M...
Certificate Number : R1-CEP 2014-327 - Rev 00
Status : Valid
Issue Date : 2021-03-05
Type : Chemical
Substance Number : 1653
Potassium Clavulanate, Diluted, With Silica, Col...
Certificate Number : R1-CEP 2014-329 - Rev 00
Status : Valid
Issue Date : 2021-03-03
Type : Chemical
Substance Number : 1653
24
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.
A AUGMENTIN ES-600-1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AUGMENTIN ES-600-1, including repackagers and relabelers. The FDA regulates AUGMENTIN ES-600-1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AUGMENTIN ES-600-1 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 ES-600-1 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A AUGMENTIN ES-600-1 supplier is an individual or a company that provides AUGMENTIN ES-600-1 active pharmaceutical ingredient (API) or AUGMENTIN ES-600-1 finished formulations upon request. The AUGMENTIN ES-600-1 suppliers may include AUGMENTIN ES-600-1 API manufacturers, exporters, distributors and traders.
click here to find a list of AUGMENTIN ES-600-1 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A AUGMENTIN ES-600-1 CEP of the European Pharmacopoeia monograph is often referred to as a AUGMENTIN ES-600-1 Certificate of Suitability (COS). The purpose of a AUGMENTIN ES-600-1 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of AUGMENTIN ES-600-1 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of AUGMENTIN ES-600-1 to their clients by showing that a AUGMENTIN ES-600-1 CEP has been issued for it. The manufacturer submits a AUGMENTIN ES-600-1 CEP (COS) as part of the market authorization procedure, and it takes on the role of a AUGMENTIN ES-600-1 CEP holder for the record. Additionally, the data presented in the AUGMENTIN ES-600-1 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the AUGMENTIN ES-600-1 DMF.
A AUGMENTIN ES-600-1 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. AUGMENTIN ES-600-1 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 ES-600-1 suppliers with CEP (COS) on PharmaCompass.
We have 9 companies offering AUGMENTIN ES-600-1
Get in contact with the supplier of your choice:
