DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
02 1SOLARA ACTIVE PHARMA SCIENCES LIMITED Chennai IN
01 2Nizatidine
01 2India
01 2Valid
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Certificate Number : R1-CEP 2002-027 - Rev 06
Status : Valid
Issue Date : 2023-04-24
Type : Chemical
Substance Number : 1453
Certificate Number : CEP 2000-083 - Rev 10
Status : Valid
Issue Date : 2023-12-19
Type : Chemical
Substance Number : 1453
A Nizatidine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nizatidine, including repackagers and relabelers. The FDA regulates Nizatidine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nizatidine 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 Nizatidine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nizatidine supplier is an individual or a company that provides Nizatidine active pharmaceutical ingredient (API) or Nizatidine finished formulations upon request. The Nizatidine suppliers may include Nizatidine API manufacturers, exporters, distributors and traders.
click here to find a list of Nizatidine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Nizatidine CEP of the European Pharmacopoeia monograph is often referred to as a Nizatidine Certificate of Suitability (COS). The purpose of a Nizatidine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Nizatidine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Nizatidine to their clients by showing that a Nizatidine CEP has been issued for it. The manufacturer submits a Nizatidine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Nizatidine CEP holder for the record. Additionally, the data presented in the Nizatidine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Nizatidine DMF.
A Nizatidine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Nizatidine 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 Nizatidine suppliers with CEP (COS) on PharmaCompass.
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