DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
02 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
03 1FORMOSA LABORATORIES, INC. Taoyuan TW
04 1HETERO DRUGS LIMITED Hyderabad IN
05 1LAURUS LABS LIMITED Hyderabad IN
06 1LAURUS LABS PRIVATE LIMITED Hyderabad IN
07 1MACLEODS PHARMACEUTICALS LIMITED Mumbai IN
08 2MELODY HEALTHCARE PVT. LTD. Boisar IN
09 1MOREPEN LABORATORIES LIMITED Baddi IN
10 1MSN PHARMACHEM PRIVATE LIMITED Pashamylaram Village IN
11 1SHANDONG NEW TIME PHARMACEUTICAL CO., LTD. Linyi CN
12 2TAPI NL B.V. Amsterdam NL
13 2TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN
14 2UNIMARK REMEDIES LIMITED Mumbai IN
15 1ZHEJIANG TIANYU PHARMACEUTICAL CO., LTD. Taizhou City CN
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Certificate Number : R1-CEP 2012-115 - Rev 03
Status : Valid
Issue Date : 2023-07-12
Type : Chemical
Substance Number : 2583
22
PharmaCompass offers a list of Montelukast Sodium 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 Montelukast Sodium manufacturer or Montelukast Sodium supplier for your needs.
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A CAS-151767-02-1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CAS-151767-02-1, including repackagers and relabelers. The FDA regulates CAS-151767-02-1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CAS-151767-02-1 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A CAS-151767-02-1 supplier is an individual or a company that provides CAS-151767-02-1 active pharmaceutical ingredient (API) or CAS-151767-02-1 finished formulations upon request. The CAS-151767-02-1 suppliers may include CAS-151767-02-1 API manufacturers, exporters, distributors and traders.
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A CAS-151767-02-1 CEP of the European Pharmacopoeia monograph is often referred to as a CAS-151767-02-1 Certificate of Suitability (COS). The purpose of a CAS-151767-02-1 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of CAS-151767-02-1 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of CAS-151767-02-1 to their clients by showing that a CAS-151767-02-1 CEP has been issued for it. The manufacturer submits a CAS-151767-02-1 CEP (COS) as part of the market authorization procedure, and it takes on the role of a CAS-151767-02-1 CEP holder for the record. Additionally, the data presented in the CAS-151767-02-1 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the CAS-151767-02-1 DMF.
A CAS-151767-02-1 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. CAS-151767-02-1 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 CAS-151767-02-1 suppliers with CEP (COS) on PharmaCompass.
We have 13 companies offering CAS-151767-02-1
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