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01 Cadila Healthcare Limited (1)
02 Hetero Labs Limited (1)
03 Mylan Laboratories Limited (1)
04 Sicor Societa (') Italiana Corticosteroidi S. r. l. (1)
05 Syn-Tech Chem. & Pharm. Co. , Ltd. (1)
06 Tateyama Kasei Co., Ltd. (1)
01 Atomoxetine Hydrochloride (2)
02 Atomoxetine hydrochloride (2)
03 Atomoxetine hydrochloride (1)
04 Atomoxetine hydrochloride "Tateyama" (1)
01 India (2)
02 Italy (1)
03 Japan (1)
04 Taiwan (1)
05 U.S.A (1)
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PharmaCompass offers a list of Atomoxetin 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 Atomoxetin Hydrochloride manufacturer or Atomoxetin Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Atomoxetin Hydrochloride manufacturer or Atomoxetin Hydrochloride supplier.
PharmaCompass also assists you with knowing the Atomoxetin Hydrochloride API Price utilized in the formulation of products. Atomoxetin Hydrochloride API Price is not always fixed or binding as the Atomoxetin Hydrochloride Price is obtained through a variety of data sources. The Atomoxetin Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A AM20060733 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AM20060733, including repackagers and relabelers. The FDA regulates AM20060733 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AM20060733 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 AM20060733 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A AM20060733 supplier is an individual or a company that provides AM20060733 active pharmaceutical ingredient (API) or AM20060733 finished formulations upon request. The AM20060733 suppliers may include AM20060733 API manufacturers, exporters, distributors and traders.
click here to find a list of AM20060733 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 AM20060733 Drug Master File in Japan (AM20060733 JDMF) empowers AM20060733 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 AM20060733 JDMF during the approval evaluation for pharmaceutical products. At the time of AM20060733 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 AM20060733 suppliers with JDMF on PharmaCompass.
We have 6 companies offering AM20060733
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