DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1M/s Dr. Reddy's Laboratories
02 1Solara Active Pharma Sciences Limited
01 1Nizatidine USP/BP/EP
02 1Nizatidine USP/Ph. Eur
01 1WC-0067
02 1WC-0127
01 2India
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Date of Issue : 2022-06-17
Valid Till : 2025-07-07
Written Confirmation Number : WC-0067
Address of the Firm : Chemical Technical Operations Unit-VI, APIIC Industrial Estate, Pydibhimavaram V...
Date of Issue : 2022-09-30
Valid Till : 2025-08-04
Written Confirmation Number : WC-0127
Address of the Firm : A1/B, SIPCOT Industrial Complex, Kudikadu, Cuddalore-607 005
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 written confirmation (Nizatidine WC) is an official document issued by a regulatory agency to a Nizatidine manufacturer, verifying that the manufacturing facility of a Nizatidine active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Nizatidine APIs or Nizatidine finished pharmaceutical products to another nation, regulatory agencies frequently require a Nizatidine WC (written confirmation) as part of the regulatory process.
click here to find a list of Nizatidine suppliers with Written Confirmation (WC) on PharmaCompass.
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