Market Place
Upload your Marketing & Sales content on your company Virtual Booth, click HERE
X
Please Wait
Applying Filters...
01 APOTEX PHARMACHEM INC. Brantford CA (1)
02 BIOCON LIMITED Bangalore IN (1)
03 BIOCON LIMITED Bengaluru IN (1)
04 CONCORD BIOTECH LIMITED Ahmedabad IN (1)
05 Chunghwa Chemical Synthesis & Biotech Co., Ltd. Shu-Lin TW (1)
06 DAIICHI SANKYO CO., LTD. Tokyo JP (1)
07 KYOWA HAKKO BIO CO., LTD. Tokyo JP (1)
08 LEK PHARMACEUTICALS D.D. Ljubljana SI (1)
09 LIVZON NEW NORTH RIVER PHARMACEUTICAL CO., LTD. Qingyuan City CN (1)
10 Ranbaxy Laboratories Limited Gurgaon IN (1)
11 TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL (1)
12 Zhejiang Hisun Pharmaceutical Co., Ltd. Taizhou City CN (1)
01 Pravastatin sodium (11)
02 Pravastatin sodium, Product Code 8000070 (1)
01 Canada (1)
02 China (2)
03 India (4)
04 Israel (1)
05 Japan (2)
06 Slovenia (1)
07 Taiwan (1)
01 Expired (1)
02 Valid (9)
03 Withdrawn by Holder (2)
77
PharmaCompass offers a list of Pravastatin 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 Pravastatin manufacturer or Pravastatin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pravastatin manufacturer or Pravastatin supplier.
PharmaCompass also assists you with knowing the Pravastatin API Price utilized in the formulation of products. Pravastatin API Price is not always fixed or binding as the Pravastatin Price is obtained through a variety of data sources. The Pravastatin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tox21_300270 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_300270, including repackagers and relabelers. The FDA regulates Tox21_300270 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_300270 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 Tox21_300270 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tox21_300270 supplier is an individual or a company that provides Tox21_300270 active pharmaceutical ingredient (API) or Tox21_300270 finished formulations upon request. The Tox21_300270 suppliers may include Tox21_300270 API manufacturers, exporters, distributors and traders.
click here to find a list of Tox21_300270 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tox21_300270 CEP of the European Pharmacopoeia monograph is often referred to as a Tox21_300270 Certificate of Suitability (COS). The purpose of a Tox21_300270 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Tox21_300270 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Tox21_300270 to their clients by showing that a Tox21_300270 CEP has been issued for it. The manufacturer submits a Tox21_300270 CEP (COS) as part of the market authorization procedure, and it takes on the role of a Tox21_300270 CEP holder for the record. Additionally, the data presented in the Tox21_300270 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Tox21_300270 DMF.
A Tox21_300270 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Tox21_300270 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 Tox21_300270 suppliers with CEP (COS) on PharmaCompass.
We have 11 companies offering Tox21_300270
Get in contact with the supplier of your choice:
