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List of Certificates of Suitability (CEPs) for Candesartan Cilexetil Active Pharmaceutical Ingredient (API) issued by the EDQM. Original Data: EDQM Database

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01 ALEMBIC PHARMACEUTICALS LIMITED Vadodara IN (1)

02 AUROBINDO PHARMA LIMITED Hyderabad IN (2)

03 CADILA HEALTHCARE LIMITED Ankleshwar IN (1)

04 CHROMO LABORATORIES INDIA PRIVATE LIMITED Pashamylaram IN (1)

05 DR. REDDY'S LABORATORIES LIMITED Hyderabad IN (1)

06 HETERO LABS LIMITED Hyderabad IN (1)

07 JUBILANT PHARMOVA LIMITED Nanjangud IN (1)

08 Jiangxi Synergy Pharmaceutical Co., Ltd. Fengxin CN (1)

09 KRKA, d.d., Novo mesto Novo mesto SI (1)

10 MACLEODS PHARMACEUTICALS LIMITED Mumbai IN (1)

11 MYLAN LABORATORIES LIMITED Hyderabad IN (2)

12 QUIMICA SINTETICA S.A. Alcala De Henares ES (1)

13 SMILAX LABORATORIES LIMITED Hyderabad IN (1)

14 SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN (2)

15 TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL (2)

16 ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. Linhai CN (1)

17 ZHEJIANG TIANYU PHARMACEUTICAL CO., LTD. Taizhou City CN (1)

18 ZHUHAI RUNDU PHARMACEUTICAL CO., LTD. Sanzao Town CN (2)

19 Zhejiang Kinglyuan Pharmaceutical Co., Ltd. Shangyu CN (1)

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01 Candesartan cilexetil (16)

02 Candesartan cilexetil, - (1)

03 Candesartan cilexetil, Form I (1)

04 Candesartan cilexetil, Form I - process 2 (1)

05 Candesartan cilexetil, Process 2 (1)

06 Candesartan cilexetil, Process II (2)

07 Candesartan cilexetil, Process-2 (1)

08 Candesartan cilexetil, Process-IV (1)

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01 China (6)

02 India (12)

03 Israel (2)

04 Slovenia (1)

05 Spain (1)

06 U.S.A (2)

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01 Expired (1)

02 Valid (16)

03 Withdrawn by Holder (7)

URL Supplier Web Content
R1-CEP 2011-266 - Rev 05
Valid
Chemical
2023-05-12
2573
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CEP 2013-007 - Rev 03
Valid
Chemical
2023-09-20
2573
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CEP 2016-132 - Rev 01
Valid
Chemical
2024-02-19
2573
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R1-CEP 2014-042 - Rev 01
Valid
Chemical
2023-01-16
2573
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R1-CEP 2013-228 - Rev 02
Valid
Chemical
2020-06-11
2573
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R1-CEP 2011-248 - Rev 02
Valid
Chemical
2021-11-22
2573
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R0-CEP 2020-164 - Rev 01
Valid
Chemical
2021-11-22
2573
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R1-CEP 2011-259 - Rev 05
Valid
Chemical
2022-06-22
2573
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R1-CEP 2013-314 - Rev 01
Valid
Chemical
2021-01-25
2573
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R0-CEP 2023-096 - Rev 00
Valid
Chemical
2023-05-19
2573
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Looking for 145040-37-5 / Candesartan Cilexetil API manufacturers, exporters & distributors?

Candesartan Cilexetil manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Candesartan Cilexetil

Synonyms

145040-37-5, Atacand, Tcv-116, Amias, Parapres, Kenzen

Cas Number

145040-37-5

Unique Ingredient Identifier (UNII)

R85M2X0D68

About Candesartan Cilexetil

Candesartan Cilexetil is a synthetic, benzimidazole-derived angiotensin II receptor antagonist prodrug with antihypertensive activity. After hydrolysis of candesartan cilexetil to candesartan during gastrointestinal absorption, candesartan selectively competes with angiotensin II for the binding of the angiotensin II receptor subtype 1 (AT1) in vascular smooth muscle, blocking angiotensin II-mediated vasoconstriction and inducing vasodilatation. In addition, antagonism of AT1 in the adrenal gland inhibits angiotensin II-stimulated aldosterone synthesis and secretion by the adrenal cortex; sodium and water excretion increase, followed by a reduction in plasma volume and blood pressure.

Candesartan Cilexetil Manufacturers

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

Candesartan Cilexetil Suppliers

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

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

Candesartan Cilexetil CEP

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

A Candesartan Cilexetil CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Candesartan Cilexetil 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 Candesartan Cilexetil suppliers with CEP (COS) on PharmaCompass.

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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