01 1BrightGene Pharmaceutical Co. Ltd.
02 1BrightGene Pharmaceutical Co. Ltd. @BrightGene Pharmaceutical Co. Ltd.
01 1Kyungbo Pharmaceutical Co., Ltd.
02 1Otran Korea Co., Ltd.
01 1Entecavir hydrate
02 1Entecavir monohydrate (micronized)
01 1China
02 1South Korea
Entecavir monohydrate (micronized)
Registrant Name : Otran Korea Co., Ltd.
Registration Date : 2022-05-30
Registration Number : No. 695-7-ND
Manufacturer Name : BrightGene Pharmaceutical Co...
Manufacturer Address : Building C25-C28, No.218 Xinghu Road, Suzhou Industrial Park, Suzhou, Jiangsu, 215123...
Registrant Name : Kyungbo Pharmaceutical Co., Ltd.
Registration Date : 2019-10-30
Registration Number : 1673-31-ND
Manufacturer Name : BrightGene Pharmaceutical Co...
Manufacturer Address : 174 Silok-ro, Asan-si, Chungcheongnam-do @Building C25-C28, No.218 Xinghu Road, Suzho...
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PharmaCompass offers a list of Entecavir Monohydrate 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 Entecavir Monohydrate manufacturer or Entecavir Monohydrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Entecavir Monohydrate manufacturer or Entecavir Monohydrate supplier.
PharmaCompass also assists you with knowing the Entecavir Monohydrate API Price utilized in the formulation of products. Entecavir Monohydrate API Price is not always fixed or binding as the Entecavir Monohydrate Price is obtained through a variety of data sources. The Entecavir Monohydrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A MP-1495 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MP-1495, including repackagers and relabelers. The FDA regulates MP-1495 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MP-1495 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 MP-1495 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A MP-1495 supplier is an individual or a company that provides MP-1495 active pharmaceutical ingredient (API) or MP-1495 finished formulations upon request. The MP-1495 suppliers may include MP-1495 API manufacturers, exporters, distributors and traders.
click here to find a list of MP-1495 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 MP-1495 Drug Master File in Korea (MP-1495 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of MP-1495. The MFDS reviews the MP-1495 KDMF as part of the drug registration process and uses the information provided in the MP-1495 KDMF to evaluate the safety and efficacy of the drug.
After submitting a MP-1495 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 MP-1495 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of MP-1495 suppliers with KDMF on PharmaCompass.
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