Market Place
Hubei Gedian Humanwell focuses on R&D, production, & sales of fertility regulation drugs & steroidal APIs. 
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01 Hubei Gedian Humanwell Pharmaceutical (1)
02 Polpharma (1)
03 Ami Lifesciences Private Limited (1)
04 Amoli Organics (1)
05 Archimica (1)
06 Aurore Life Sciences (1)
07 CTX Lifesciences (2)
08 Corden Pharma Bergamo S.p.A (1)
09 Dasami Lab (2)
10 ERREDUE S.P.A. IT 24040 Isso (1)
11 F.I.S. Fabbrica Italiana Sintetici (2)
12 Glenmark Life Sciences (1)
13 Jubilant Generics (2)
14 KONDUSKAR LABORATORIES PVT LTD (1)
15 MATRIX LABORATORIES XIAMEN LTD. (1)
16 MSN Laboratories (1)
17 Siegfried AG (1)
18 Signa S.A. de C.V. (1)
19 Sun Pharmaceutical Industries Limited (1)
20 Taro Pharmaceutical Industries (1)
21 Trifarma (1)
22 Zhejiang Jiuzhou Pharmaceutical (2)
01 OXCARBAZEPHIN USP (1)
02 OXCARBAZEPINE (14)
03 OXCARBAZEPINE CO-PRECIPITATE (1)
04 OXCARBAZEPINE MICRONIZED (1)
05 OXCARBAZEPINE USP (9)
06 OXCARBAZEPINE USP (PROCESS-II) (1)
01 China (4)
02 India (13)
03 Italy (6)
04 Mexico (1)
05 Poland (1)
06 Switzerland (1)
07 U.S.A (1)
01 Active (19)
02 Inactive (8)
01 Complete (14)
02 Blank (13)
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PharmaCompass offers a list of Oxcarbazepine 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 Oxcarbazepine manufacturer or Oxcarbazepine supplier for your needs.
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PharmaCompass also assists you with knowing the Oxcarbazepine API Price utilized in the formulation of products. Oxcarbazepine API Price is not always fixed or binding as the Oxcarbazepine Price is obtained through a variety of data sources. The Oxcarbazepine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A MolPort-001-685-316 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-685-316, including repackagers and relabelers. The FDA regulates MolPort-001-685-316 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-685-316 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 MolPort-001-685-316 supplier is an individual or a company that provides MolPort-001-685-316 active pharmaceutical ingredient (API) or MolPort-001-685-316 finished formulations upon request. The MolPort-001-685-316 suppliers may include MolPort-001-685-316 API manufacturers, exporters, distributors and traders.
click here to find a list of MolPort-001-685-316 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A MolPort-001-685-316 DMF (Drug Master File) is a document detailing the whole manufacturing process of MolPort-001-685-316 active pharmaceutical ingredient (API) in detail. Different forms of MolPort-001-685-316 DMFs exist exist since differing nations have different regulations, such as MolPort-001-685-316 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A MolPort-001-685-316 DMF submitted to regulatory agencies in the US is known as a USDMF. MolPort-001-685-316 USDMF includes data on MolPort-001-685-316's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The MolPort-001-685-316 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of MolPort-001-685-316 suppliers with USDMF on PharmaCompass.
We have 22 companies offering MolPort-001-685-316
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