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01 APOTECNIA S. A. (1)
02 Amino Chemicals Ltd. (1)
03 Aurobindo Pharma Limited (1)
04 Derivados Quimicos sau (4)
05 ERCROS INDUSTRIAL,S. A. (1)
06 GEDEON RICHTER Plc. (1)
07 Hetero Labs Limited (1)
08 INIST ST CO. , LTD. (1)
09 Permakem Asia Co., Ltd. (1)
10 Qilu Pharmaceutical Co. , Ltd. (1)
11 Shandong Anhong Pharmaceutical Co. , Ltd. (1)
12 Spera Nexus Co., Ltd. (1)
13 Synergene Active Ingredients Pvt. Ltd. (1)
14 Uquifa Mexico, S. A. de C. V. (1)
15 Wavelength Enterprises Ltd (1)
01 Terbinafine HCl (1)
02 Terbinafine Hydrochloride (5)
03 Terbinafine hydrochloride (12)
01 China (2)
02 France (1)
03 Gabon (1)
04 Hungary (1)
05 India (3)
06 Japan (2)
07 Malta (1)
08 South Korea (1)
09 Spain (6)
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PharmaCompass offers a list of Terbinafine 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 Terbinafine Hydrochloride manufacturer or Terbinafine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Terbinafine Hydrochloride manufacturer or Terbinafine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Terbinafine Hydrochloride API Price utilized in the formulation of products. Terbinafine Hydrochloride API Price is not always fixed or binding as the Terbinafine Hydrochloride Price is obtained through a variety of data sources. The Terbinafine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A MolPort-001-758-011 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-758-011, including repackagers and relabelers. The FDA regulates MolPort-001-758-011 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-758-011 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-001-758-011 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A MolPort-001-758-011 supplier is an individual or a company that provides MolPort-001-758-011 active pharmaceutical ingredient (API) or MolPort-001-758-011 finished formulations upon request. The MolPort-001-758-011 suppliers may include MolPort-001-758-011 API manufacturers, exporters, distributors and traders.
click here to find a list of MolPort-001-758-011 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 MolPort-001-758-011 Drug Master File in Japan (MolPort-001-758-011 JDMF) empowers MolPort-001-758-011 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 MolPort-001-758-011 JDMF during the approval evaluation for pharmaceutical products. At the time of MolPort-001-758-011 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 MolPort-001-758-011 suppliers with JDMF on PharmaCompass.
We have 14 companies offering MolPort-001-758-011
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