01 1Cambrex Profarmaco Milano Srl
02 1Syn-Tech Chem & Pharm. Co., Ltd.
01 1Hyons Co., Ltd.
02 1Samoh Pharmaceutical Co., Ltd.
01 2Epinephrine tartrate
01 1Taiwan
02 1U.S.A
Registrant Name : Samoh Pharmaceutical Co., Ltd.
Registration Date : 2019-09-05
Registration Number : 20190905-210-J-425
Manufacturer Name : Cambrex Profarmaco Milano Sr...
Manufacturer Address : 20067, Via Curiel, 34, Paullo (MI), ITALY
Registrant Name : Hyons Co., Ltd.
Registration Date : 2021-05-17
Registration Number : 20210517-210-J-993
Manufacturer Name : Syn-Tech Chem & Pharm. Co., ...
Manufacturer Address : No. 168, Kai Yuan Rd., Hsin-Ying, Tainan City 73055, Taiwan
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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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A LIGNOSPAN FORTE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LIGNOSPAN FORTE, including repackagers and relabelers. The FDA regulates LIGNOSPAN FORTE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LIGNOSPAN FORTE 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 LIGNOSPAN FORTE supplier is an individual or a company that provides LIGNOSPAN FORTE active pharmaceutical ingredient (API) or LIGNOSPAN FORTE finished formulations upon request. The LIGNOSPAN FORTE suppliers may include LIGNOSPAN FORTE API manufacturers, exporters, distributors and traders.
click here to find a list of LIGNOSPAN FORTE suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a LIGNOSPAN FORTE Drug Master File in Korea (LIGNOSPAN FORTE KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of LIGNOSPAN FORTE. The MFDS reviews the LIGNOSPAN FORTE KDMF as part of the drug registration process and uses the information provided in the LIGNOSPAN FORTE KDMF to evaluate the safety and efficacy of the drug.
After submitting a LIGNOSPAN FORTE KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their LIGNOSPAN FORTE API can apply through the Korea Drug Master File (KDMF).
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