01 Dr. Reddy's Laboratories (1)
02 Apotex Pharmachem (1)
03 Aurobindo Pharma Limited (1)
04 Cadila Pharmaceuticals (1)
05 Glenmark Life Sciences (1)
06 Hetero Drugs (1)
07 MSN Laboratories (1)
08 Macleods Pharmaceuticals Limited (1)
09 Olon S.p.A (1)
10 SCI PHARMTECH (1)
11 Sun Pharmaceutical Industries Limited (1)
12 Teva API (1)
13 Unichem Laboratories Limited (1)
14 Viatris (1)
15 ZCL Chemicals Limited (1)
16 Zhejiang Jiuzhou Pharmaceutical (1)
17 Zydus Lifesciences (1)
01 ATOMOXETINE HCL USP (1)
02 ATOMOXETINE HYDROCHLORIDE (5)
03 ATOMOXETINE HYDROCHLORIDE DRUG SUBSTANCE (1)
04 ATOMOXETINE HYDROCHLORIDE USP (9)
05 ATOMOXETINE HYDROCHLORIDE USP [ROUTE CODE "MY"] (1)
01 Canada (1)
02 China (1)
03 India (11)
04 Israel (1)
05 Italy (1)
06 Taiwan (1)
07 U.S.A (1)
01 Active (15)
02 Inactive (2)
01 Complete (8)
02 Blank (9)
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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.
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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.
A AM20060733 DMF (Drug Master File) is a document detailing the whole manufacturing process of AM20060733 active pharmaceutical ingredient (API) in detail. Different forms of AM20060733 DMFs exist exist since differing nations have different regulations, such as AM20060733 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A AM20060733 DMF submitted to regulatory agencies in the US is known as a USDMF. AM20060733 USDMF includes data on AM20060733's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The AM20060733 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of AM20060733 suppliers with USDMF on PharmaCompass.
We have 17 companies offering AM20060733
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