DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr. Reddy's Laboratories Ltd.
02 1Ohara Pharmaceutical Co., Ltd.
03 1Solara Active Pharma Sciences Limited
01 1Japanese Pharmacopoeia nizatidine (production only)
02 1NIZATIDINE
03 1Nizatidine
01 2India
02 1Japan
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Registration Number : 218MF10215
Registrant's Address : 8-2-337, Road No. 3, Banjara Hills, Hyderabad 500 034, TELANGANA, INDIA
Initial Date of Registration : 2006-02-16
Latest Date of Registration : 2022-01-11
Japanese Pharmacopoeia Nizatidine (for manufacturing only)
Registration Number : 220MF10171
Registrant's Address : 121-15 Torino, Koka-cho, Koka City, Shiga Prefecture
Initial Date of Registration : 2008-07-24
Latest Date of Registration : 2008-07-24
Registration Number : 223MF10080
Registrant's Address : The Batra Center, No. 28, Sardar Patel Road, Guindy, Chennai 600 032. India
Initial Date of Registration : 2011-06-15
Latest Date of Registration : 2011-06-15
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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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nizatidine manufacturer or Nizatidine supplier.
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.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Tazac;Axid;Axid AR Drug Master File in Japan (Tazac;Axid;Axid AR JDMF) empowers Tazac;Axid;Axid AR API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Tazac;Axid;Axid AR JDMF during the approval evaluation for pharmaceutical products. At the time of Tazac;Axid;Axid AR JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Tazac;Axid;Axid AR suppliers with JDMF on PharmaCompass.
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