01 1CIPLA LIMITED Mumbai IN
02 1Unichem Laboratories Limited Mumbai IN
01 1Nateglinide
02 1Nateglinide, Form H
01 2India
01 1Valid
02 1Withdrawn by Holder
Certificate Number : R0-CEP 2015-308 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2017-06-08
Type : Chemical
Substance Number : 2575
Certificate Number : CEP 2015-134 - Rev 01
Status : Valid
Issue Date : 2024-11-12
Type : Chemical
Substance Number : 2575
36
PharmaCompass offers a list of Nateglinide 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 Nateglinide manufacturer or Nateglinide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nateglinide manufacturer or Nateglinide supplier.
PharmaCompass also assists you with knowing the Nateglinide API Price utilized in the formulation of products. Nateglinide API Price is not always fixed or binding as the Nateglinide Price is obtained through a variety of data sources. The Nateglinide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A N0912 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of N0912, including repackagers and relabelers. The FDA regulates N0912 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. N0912 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 N0912 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A N0912 supplier is an individual or a company that provides N0912 active pharmaceutical ingredient (API) or N0912 finished formulations upon request. The N0912 suppliers may include N0912 API manufacturers, exporters, distributors and traders.
click here to find a list of N0912 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A N0912 CEP of the European Pharmacopoeia monograph is often referred to as a N0912 Certificate of Suitability (COS). The purpose of a N0912 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of N0912 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of N0912 to their clients by showing that a N0912 CEP has been issued for it. The manufacturer submits a N0912 CEP (COS) as part of the market authorization procedure, and it takes on the role of a N0912 CEP holder for the record. Additionally, the data presented in the N0912 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the N0912 DMF.
A N0912 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. N0912 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 N0912 suppliers with CEP (COS) on PharmaCompass.
We have 2 companies offering N0912
Get in contact with the supplier of your choice:
