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01 1Interquim, S.A. Sant Cugat Del Vallès ES

02 2TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL

03 1ALEMBIC PHARMACEUTICALS LIMITED Vadodara IN

04 2AMOLI ORGANICS PRIVATE LIMITED Mumbai IN

05 2APITORIA PHARMA PRIVATE LIMITED Hyderabad IN

06 1APOTEX PHARMACHEM INDIA PVT. LTD Bangalore IN

07 1CADILA PHARMACEUTICALS LIMITED Ankleshwar IN

08 1CHROMO LABORATORIES INDIA PRIVATE LIMITED Pashamylaram IN

09 1CIPLA LIMITED Mumbai IN

10 1CPL PHARMACEUTICALS PRIVATE LIMITED Ahmedabad IN

11 1DAIICHI SANKYO CO., LTD. Tokyo JP

12 1DONG BANG FUTURE TECH & LIFE CO., LTD. Hwaseong-si KR

13 1DR. REDDY'S LABORATORIES LIMITED Hyderabad IN

14 1EUROAPI HUNGARY Ltd. Budapest HU

15 2GLENMARK LIFE SCIENCES LIMITED Mumbai IN

16 1HEC PHARM CO., LTD. Yidu City CN

17 1HETERO LABS LIMITED Hyderabad IN

18 1HIKAL LIMITED Bangalore IN

19 1JUBILANT PHARMOVA LIMITED Nanjangud IN

20 1KRKA, d.d., Novo mesto Novo mesto SI

21 1LUPIN LIMITED Mumbai IN

22 1MACLEODS PHARMACEUTICALS LIMITED Mumbai IN

23 1MICRO LABS LIMITED Bengaluru IN

24 1MOREPEN LABORATORIES LIMITED Baddi IN

25 1MSN LABORATORIES PRIVATE LIMITED Rudraram Village IN

26 1SECOND PHARMA CO., LTD. Shangyu City CN

27 1SHANDONG ANXIN PHARMACEUTICAL CO., LTD. Dongjia Town CN

28 1SINTENOVO S.A. DE C.V. Barcelona ES

29 1TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN

30 1TORRENT PHARMACEUTICALS LIMITED Ahmedabad IN

31 1Unichem Laboratories Limited Mumbai IN

32 1VASUDHA PHARMA CHEM LIMITED Hyderabad IN

33 1VENKATA NARAYANA ACTIVE INGREDIENTS PRIVATE LIMITED Chennai IN

34 2ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. Linhai CN

35 2ZHEJIANG TIANYU PHARMACEUTICAL CO., LTD. Taizhou City CN

36 1ZHUHAI RUNDU PHARMACEUTICAL CO., LTD. Sanzao Town CN

37 1ZYDUS LIFESCIENCES LIMITED Vadodara IN

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PharmaCompass
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothInterquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.

R1-CEP 2014-295 - Rev 01
Valid
Chemical
2022-12-19
2600
Interquim

01

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PharmaVenue
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothInterquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.

Olmesartan Medoxomil

Certificate Number : R1-CEP 2014-295 - Rev 01

Status : Valid

Issue Date : 2022-12-19

Type : Chemical

Substance Number : 2600

Interquim
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothTAPI offers customized CDMO Solutions for API development and manufacturing services.

R1-CEP 2012-170 - Rev 01
Valid
Chemical
2022-05-25
2600
TAPI Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothTAPI offers customized CDMO Solutions for API development and manufacturing services.

Olmesartan Medoxomil

Certificate Number : R1-CEP 2012-170 - Rev 01

Status : Valid

Issue Date : 2022-05-25

Type : Chemical

Substance Number : 2600

TAPI Company Banner

Olmesartan Manufacturers

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

Olmesartan Suppliers

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

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

Olmesartan CEP

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

A Olmesartan CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Olmesartan 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 Olmesartan 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.