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01 1CIPAN - Companhia Industrial Produtora de Antibióticos, SA
02 1Zhejiang Changhai Pharmaceuticals Co.,Ltd.
01 1Ace Biopharm Co., Ltd.
02 1Samoh Pharmaceutical Co., Ltd.
01 2Minocycline hydrochloride
01 1China
02 1Spain
Registrant Name : Samoh Pharmaceutical Co., Ltd.
Registration Date : 2024-01-31
Registration Number : 20240131-211-J-1572
Manufacturer Name : CIPAN - Companhia Industrial...
Manufacturer Address : Rua da Estação, 1/1A, 2600-726 Castanheira do Ribatejo, Portugal
Registrant Name : Ace Biopharm Co., Ltd.
Registration Date : 2022-09-05
Registration Number : 20220905-211-J-1355
Manufacturer Name : Zhejiang Changhai Pharmaceut...
Manufacturer Address : 188 Mid Zhiyuan Avenue, Binhai New Area, Shaoxing City, Zhejiang Province, 312366, PR...
A Minocycline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Minocycline, including repackagers and relabelers. The FDA regulates Minocycline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Minocycline 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 Minocycline manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Minocycline supplier is an individual or a company that provides Minocycline active pharmaceutical ingredient (API) or Minocycline finished formulations upon request. The Minocycline suppliers may include Minocycline API manufacturers, exporters, distributors and traders.
click here to find a list of Minocycline 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 Minocycline Drug Master File in Korea (Minocycline KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Minocycline. The MFDS reviews the Minocycline KDMF as part of the drug registration process and uses the information provided in the Minocycline KDMF to evaluate the safety and efficacy of the drug.
After submitting a Minocycline 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 Minocycline API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Minocycline suppliers with KDMF on PharmaCompass.
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