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01 NEULAND LABORATORIES LIMITED Hyderabad IN (3)
02 SHODHANA LABORATORIES PRIVATE LIMITED Hyderabad IN (1)
03 APITORIA PHARMA PRIVATE LIMITED Hyderabad IN (2)
04 CIPLA LIMITED Mumbai IN (1)
05 DR. REDDY'S LABORATORIES LIMITED Hyderabad IN (1)
06 HETERO LABS LIMITED Hyderabad IN (2)
07 JUBILANT PHARMOVA LIMITED Nanjangud IN (1)
08 MICRO LABS LIMITED Bengaluru IN (1)
09 MYLAN LABORATORIES LIMITED Hyderabad IN (2)
10 OLON S.P.A. Rodano IT (1)
11 RUYUAN HEC PHARM CO., LTD. Shaoguan CN (1)
12 ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. Linhai CN (1)
01 Escitalopram oxalate (11)
02 Escitalopram oxalate, Process I (1)
03 Escitalopram oxalate, Process II (3)
04 Escitalopram oxalate, Process-II (1)
05 Escitalopram oxalate, Process-III (1)
01 China (2)
02 India (12)
03 Italy (1)
04 U.S.A (2)
01 Valid (17)
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PharmaCompass offers a list of Escitalopram Oxalate 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 Escitalopram Oxalate manufacturer or Escitalopram Oxalate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Escitalopram Oxalate manufacturer or Escitalopram Oxalate supplier.
PharmaCompass also assists you with knowing the Escitalopram Oxalate API Price utilized in the formulation of products. Escitalopram Oxalate API Price is not always fixed or binding as the Escitalopram Oxalate Price is obtained through a variety of data sources. The Escitalopram Oxalate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Escitalopram manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Escitalopram, including repackagers and relabelers. The FDA regulates Escitalopram manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Escitalopram 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 Escitalopram manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Escitalopram supplier is an individual or a company that provides Escitalopram active pharmaceutical ingredient (API) or Escitalopram finished formulations upon request. The Escitalopram suppliers may include Escitalopram API manufacturers, exporters, distributors and traders.
click here to find a list of Escitalopram suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Escitalopram CEP of the European Pharmacopoeia monograph is often referred to as a Escitalopram Certificate of Suitability (COS). The purpose of a Escitalopram CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Escitalopram EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Escitalopram to their clients by showing that a Escitalopram CEP has been issued for it. The manufacturer submits a Escitalopram CEP (COS) as part of the market authorization procedure, and it takes on the role of a Escitalopram CEP holder for the record. Additionally, the data presented in the Escitalopram CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Escitalopram DMF.
A Escitalopram CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Escitalopram 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 Escitalopram suppliers with CEP (COS) on PharmaCompass.
We have 11 companies offering Escitalopram
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