01 1Syn-Tech Chem. & Pharm. Co. , Ltd.
02 1Viyash Life Sciences Private Limited
01 1Epinephrine Hydrogentrate
02 1Epinephrine Tartrate
01 1India
02 1Taiwan
Registration Number : 303MF10034
Registrant's Address : No. 168 Kai-Yuan Rd. , Hsin-Ying Tainan City, 73055. Taiwan
Initial Date of Registration : 2021-02-16
Latest Date of Registration : 2021-02-16
Registration Number : 307MF10050
Registrant's Address : Plot No. 290, Srivalli's Corporate, Road No. 6, Kakatiya Hills, Madhapur, Hyderabad-5...
Initial Date of Registration : 2025-04-02
Latest Date of Registration : 2025-04-02
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PharmaCompass offers a list of Epinephrine Bitartrate 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 Epinephrine Bitartrate manufacturer or Epinephrine Bitartrate supplier for your needs.
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PharmaCompass also assists you with knowing the Epinephrine Bitartrate API Price utilized in the formulation of products. Epinephrine Bitartrate API Price is not always fixed or binding as the Epinephrine Bitartrate Price is obtained through a variety of data sources. The Epinephrine Bitartrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Asthmahaler manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Asthmahaler, including repackagers and relabelers. The FDA regulates Asthmahaler manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Asthmahaler 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 Asthmahaler supplier is an individual or a company that provides Asthmahaler active pharmaceutical ingredient (API) or Asthmahaler finished formulations upon request. The Asthmahaler suppliers may include Asthmahaler API manufacturers, exporters, distributors and traders.
click here to find a list of Asthmahaler 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 Asthmahaler Drug Master File in Japan (Asthmahaler JDMF) empowers Asthmahaler 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 Asthmahaler JDMF during the approval evaluation for pharmaceutical products. At the time of Asthmahaler 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 Asthmahaler suppliers with JDMF on PharmaCompass.
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