With Virupaksha, you get a quality product with on-time delivery.
01 1VIRUPAKSHA ORGANICS LIMITED Hyderabad IN
02 3NEULAND LABORATORIES LIMITED Hyderabad IN
03 2APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
04 2CIPLA LIMITED Mumbai IN
05 1DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
06 2HETERO LABS LIMITED Hyderabad IN
07 1JUBILANT PHARMOVA LIMITED Nanjangud IN
08 2MICRO LABS LIMITED Bengaluru IN
09 1OLON S.P.A. Rodano IT
10 1RUYUAN HEC PHARM CO., LTD. Shaoguan CN
11 1SHODHANA LABORATORIES PRIVATE LIMITED Hyderabad IN
12 1SMILAX LABORATORIES LIMITED Hyderabad IN
13 2TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN
14 1VENKAR CHEMICALS PVT. LTD. Hyderabad IN
15 1ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. Linhai CN
With Virupaksha, you get a quality product with on-time delivery.
Certificate Number : CEP 2022-032 - Rev 00
Status : Valid
Issue Date : 2024-05-13
Type : Chemical
Substance Number : 2733
Neuland Laboratories- A dedicated 100% API provider.
Escitalopram Oxalate, Process-III
Certificate Number : CEP 2021-161 - Rev 02
Status : Valid
Issue Date : 2024-08-22
Type : Chemical
Substance Number : 2733
Neuland Laboratories- A dedicated 100% API provider.
Certificate Number : CEP 2017-217 - Rev 01
Status : Valid
Issue Date : 2024-08-23
Type : Chemical
Substance Number : 2733
Neuland Laboratories- A dedicated 100% API provider.
Escitalopram Oxalate, Process-II
Certificate Number : R0-CEP 2019-096 - Rev 03
Status : Withdrawn by Holder
Issue Date : 2023-03-24
Type : Chemical
Substance Number : 2733
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 13 companies offering Escitalopram
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
