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Olainfarm is one of the leading pharmaceutical companies in the Baltic States and Northern Europe, with almost 50 years of experience. 
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01 Joint Stock Company OLAIN FARM (2)
02 Alembic Pharmaceuticals Limited (1)
03 Cheer Fine Pharmaceutical Co. , Ltd. (1)
04 DNP Fine Chemical Utsunomiya Co., Ltd. (1)
05 LUPIN LIMITED. (1)
06 Procos S. p. A. (1)
07 UBE Co., Ltd. (3)
08 Zhejiang Apeloa Kangyu Pharmaceutical Co. , Ltd. (1)
01 Memantine Hydrochloride (4)
02 Memantine hydrochloride (3)
03 Memantine hydrochloride (crushed product) (2)
04 Refined memantine hydrochloride (crushed product) (2)
01 China (2)
02 India (2)
03 Italy (1)
04 Japan (4)
05 Latvia (2)
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PharmaCompass offers a list of Memantine Hydrochloride 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 Memantine Hydrochloride manufacturer or Memantine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Memantine Hydrochloride manufacturer or Memantine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Memantine Hydrochloride API Price utilized in the formulation of products. Memantine Hydrochloride API Price is not always fixed or binding as the Memantine Hydrochloride Price is obtained through a variety of data sources. The Memantine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A AM20070534 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AM20070534, including repackagers and relabelers. The FDA regulates AM20070534 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AM20070534 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 AM20070534 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A AM20070534 supplier is an individual or a company that provides AM20070534 active pharmaceutical ingredient (API) or AM20070534 finished formulations upon request. The AM20070534 suppliers may include AM20070534 API manufacturers, exporters, distributors and traders.
click here to find a list of AM20070534 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 AM20070534 Drug Master File in Japan (AM20070534 JDMF) empowers AM20070534 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 AM20070534 JDMF during the approval evaluation for pharmaceutical products. At the time of AM20070534 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 AM20070534 suppliers with JDMF on PharmaCompass.
We have 8 companies offering AM20070534
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