IOL Chemicals is an innovation-driven bulk drug, Intermediate and Specialty Chemicals company.
01 1IOL CHEMICALS AND PHARMACEUTICALS LTD Ludhiana IN
02 1ALEMBIC PHARMACEUTICALS LIMITED Vadodara IN
03 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
04 1ATUL BIOSCIENCE LIMITED Ambernath (East) IN
05 1AURORE LIFE SCIENCES PRIVATE LIMITED Hyderabad IN
06 1CIPLA LIMITED Mumbai IN
07 1DIVI'S LABORATORIES LIMITED Hyderabad IN
08 1HETERO LABS LIMITED Hyderabad IN
09 1IPCA LABORATORIES LIMITED Mumbai IN
10 2IPCA Laboratories Limited Mumbai IN
11 1JUBILANT PHARMOVA LIMITED Nanjangud IN
12 2KRKA, d.d., Novo mesto Novo mesto SI
13 2MICRO LABS LIMITED Bengaluru IN
14 1MSN LIFE SCIENCES PRIVATE LIMITED Medak IN
15 1MYLAN LABORATORIES LIMITED Hyderabad IN
16 1NINGBO MENOVO PHARMACEUTICAL CO., LTD. Ningbo CN
17 1SANECA PHARMACEUTICALS A.S. Hlohovec SK
18 1SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN
19 1SYNERGENE ACTIVE INGREDIENTS PRIVATE LIMITED Hyderabad IN
20 4TAPI NL B.V. Amsterdam NL
21 1Unichem Laboratories Limited Mumbai IN
22 1VASUDHA PHARMA CHEM LIMITED Hyderabad IN
23 1VIYASH LIFE SCIENCES PRIVATE LIMITED Hyderabad IN
24 2ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. Linhai CN
25 1ZHEJIANG MENOVO PHARMACEUTICAL CO., LTD. Shangyu City CN
26 3ZHEJIANG TIANYU PHARMACEUTICAL CO., LTD. Taizhou City CN
27 1ZHUHAI RUNDU PHARMACEUTICAL CO., LTD. Zhuhai City CN
28 1ZYDUS LIFESCIENCES LIMITED Vadodara IN
29 1Zhejiang Hisun Pharmaceutical Co., Ltd. Taizhou City CN
IOL Chemicals is an innovation-driven bulk drug, Intermediate and Specialty Chemicals company.
Certificate Number : CEP 2022-380 - Rev 00
Status : Valid
Issue Date : 2024-02-05
Type : Chemical
Substance Number : 2232
34
PharmaCompass offers a list of Losartan Potassium 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 Losartan Potassium manufacturer or Losartan Potassium supplier for your needs.
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A Neo Lotan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Neo Lotan, including repackagers and relabelers. The FDA regulates Neo Lotan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Neo Lotan API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Neo Lotan supplier is an individual or a company that provides Neo Lotan active pharmaceutical ingredient (API) or Neo Lotan finished formulations upon request. The Neo Lotan suppliers may include Neo Lotan API manufacturers, exporters, distributors and traders.
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A Neo Lotan CEP of the European Pharmacopoeia monograph is often referred to as a Neo Lotan Certificate of Suitability (COS). The purpose of a Neo Lotan CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Neo Lotan EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Neo Lotan to their clients by showing that a Neo Lotan CEP has been issued for it. The manufacturer submits a Neo Lotan CEP (COS) as part of the market authorization procedure, and it takes on the role of a Neo Lotan CEP holder for the record. Additionally, the data presented in the Neo Lotan CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Neo Lotan DMF.
A Neo Lotan CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Neo Lotan CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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We have 26 companies offering Neo Lotan
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