01 Bal Pharma Limited (2)
02 Industrias Farmaceuticas Almirall, SA@Ranke Quimica, SA_x000D_ (micronized Evastin manufacturing plant) (1)
03 RANKE QUIMICA, S.A. (1)
04 Ranke Quimica, S.A. (1)
05 STech Pharma Co., Ltd. (1)
06 Yuil Farm Tech Co., Ltd. (1)
01 Boryeong Co., Ltd. (3)
02 Kookjeon Pharmaceutical Co., Ltd. (1)
03 STech Pharma Co., Ltd. (1)
04 Sangjin Trading Co., Ltd. (1)
05 Yuil Farm Tech Co., Ltd. (1)
01 Evastin (7)
01 India (2)
02 Japan (1)
03 South Korea (1)
04 Spain (3)
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PharmaCompass offers a list of Ebastine 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 Ebastine manufacturer or Ebastine supplier for your needs.
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A MolPort-001-795-067 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-795-067, including repackagers and relabelers. The FDA regulates MolPort-001-795-067 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-795-067 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 MolPort-001-795-067 supplier is an individual or a company that provides MolPort-001-795-067 active pharmaceutical ingredient (API) or MolPort-001-795-067 finished formulations upon request. The MolPort-001-795-067 suppliers may include MolPort-001-795-067 API manufacturers, exporters, distributors and traders.
click here to find a list of MolPort-001-795-067 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 MolPort-001-795-067 Drug Master File in Korea (MolPort-001-795-067 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of MolPort-001-795-067. The MFDS reviews the MolPort-001-795-067 KDMF as part of the drug registration process and uses the information provided in the MolPort-001-795-067 KDMF to evaluate the safety and efficacy of the drug.
After submitting a MolPort-001-795-067 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 MolPort-001-795-067 API can apply through the Korea Drug Master File (KDMF).
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We have 4 companies offering MolPort-001-795-067
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