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
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PharmaCompass offers a list of Nizatidine 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 Nizatidine manufacturer or Nizatidine supplier for your needs.
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PharmaCompass also assists you with knowing the Nizatidine API Price utilized in the formulation of products. Nizatidine API Price is not always fixed or binding as the Nizatidine Price is obtained through a variety of data sources. The Nizatidine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tazac;Axid;Axid AR manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tazac;Axid;Axid AR, including repackagers and relabelers. The FDA regulates Tazac;Axid;Axid AR manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tazac;Axid;Axid AR API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Tazac;Axid;Axid AR supplier is an individual or a company that provides Tazac;Axid;Axid AR active pharmaceutical ingredient (API) or Tazac;Axid;Axid AR finished formulations upon request. The Tazac;Axid;Axid AR suppliers may include Tazac;Axid;Axid AR API manufacturers, exporters, distributors and traders.
click here to find a list of Tazac;Axid;Axid AR suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tazac;Axid;Axid AR CEP of the European Pharmacopoeia monograph is often referred to as a Tazac;Axid;Axid AR Certificate of Suitability (COS). The purpose of a Tazac;Axid;Axid AR CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Tazac;Axid;Axid AR EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Tazac;Axid;Axid AR to their clients by showing that a Tazac;Axid;Axid AR CEP has been issued for it. The manufacturer submits a Tazac;Axid;Axid AR CEP (COS) as part of the market authorization procedure, and it takes on the role of a Tazac;Axid;Axid AR CEP holder for the record. Additionally, the data presented in the Tazac;Axid;Axid AR CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Tazac;Axid;Axid AR DMF.
A Tazac;Axid;Axid AR CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Tazac;Axid;Axid AR 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 Tazac;Axid;Axid AR suppliers with CEP (COS) on PharmaCompass.
We have 2 companies offering Tazac;Axid;Axid AR
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