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Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide. 
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01 Polpharma (1)
02 Alembic Pharmaceuticals Limited (2)
03 Alkaloida Chemical Company Zrt (1)
04 Aurobindo Pharma Limited (1)
05 Cilag AG (1)
06 Cipla (1)
07 Dishman Carbogen Amcis (2)
08 Divis Laboratories (1)
09 Glenmark Life Sciences (1)
10 Hetero Drugs (1)
11 Johnson & Johnson Innovative Medicine (1)
12 Lupin Ltd (1)
13 MSN Laboratories (1)
14 Pfanstiehl (1)
15 ScinoPharm Taiwan, Ltd (1)
16 Signa S.A. de C.V. (1)
17 Sun Pharmaceutical Industries Limited (1)
18 Torrent Pharmaceuticals Limited (1)
19 Unichem Laboratories Limited (1)
20 Unimark Remedies Limited (2)
21 Zhejiang Huahai Pharmaceutical (1)
22 Zydus Lifesciences (1)
01 TOPIRAMATE (9)
02 TOPIRAMATE DRUG SUBSTANCE (1)
03 TOPIRAMATE USP (12)
04 TOPIRAMATE USP (PROCESS A) (1)
05 TOPIRAMATE USP [ROUTE CODE - "TI"] (1)
06 Topiramate (1)
01 China (1)
02 Hungary (1)
03 India (17)
04 Mexico (1)
05 Poland (1)
06 Switzerland (1)
07 Taiwan (1)
08 U.S.A (2)
01 Active (16)
02 Inactive (9)
01 Complete (11)
02 Blank (14)
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PharmaCompass offers a list of Topiramate 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 Topiramate manufacturer or Topiramate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Topiramate manufacturer or Topiramate supplier.
PharmaCompass also assists you with knowing the Topiramate API Price utilized in the formulation of products. Topiramate API Price is not always fixed or binding as the Topiramate Price is obtained through a variety of data sources. The Topiramate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A MolPort-001-615-062 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-615-062, including repackagers and relabelers. The FDA regulates MolPort-001-615-062 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-615-062 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 MolPort-001-615-062 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A MolPort-001-615-062 supplier is an individual or a company that provides MolPort-001-615-062 active pharmaceutical ingredient (API) or MolPort-001-615-062 finished formulations upon request. The MolPort-001-615-062 suppliers may include MolPort-001-615-062 API manufacturers, exporters, distributors and traders.
click here to find a list of MolPort-001-615-062 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A MolPort-001-615-062 DMF (Drug Master File) is a document detailing the whole manufacturing process of MolPort-001-615-062 active pharmaceutical ingredient (API) in detail. Different forms of MolPort-001-615-062 DMFs exist exist since differing nations have different regulations, such as MolPort-001-615-062 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A MolPort-001-615-062 DMF submitted to regulatory agencies in the US is known as a USDMF. MolPort-001-615-062 USDMF includes data on MolPort-001-615-062's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The MolPort-001-615-062 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of MolPort-001-615-062 suppliers with USDMF on PharmaCompass.
We have 22 companies offering MolPort-001-615-062
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