Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
01 1Centrient Pharmaceuticals (Zibo) Co., Ltd.
02 17ACS DOBFAR SpA
03 2China Union Chempharma (Suzhou) Co., Ltd.
04 1Hawon Precision Chemical Co., Ltd.
05 1Kyungbo Pharmaceutical Co., Ltd.
06 6LUPIN LTD
07 2Lupin LTD
08 6Lupin Limited
09 2Lupin Ltd.
10 1NCPC Hebei Huamin Pharmaceutical Co.,Ltd
11 1Qilu Antibiotics Pharmaceutical Co., Ltd
12 1Youngjin Pharmaceutical Co., Ltd.
13 4Zhejiang Anglikang Pharmaceutical Co., Ltd.
14 9Zhejiang Dongbang Pharmaceutical Co., Ltd
15 3Zhejiang Dongbang Pharmaceutical Co., Ltd.
16 1Zhejiang Dongbang Pharmaceutical Co.,Ltd.
Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
Registrant Name : Aging Life Science Co., Ltd.
Registration Date : 2017-04-11
Registration Number : 20170411-20-A-326-20
Manufacturer Name : Centrient Pharmaceuticals (Z...
Manufacturer Address : West of Baoshan Road, North of Beiling Road, High-Tech Zone, Zibo Shandong Province, ...
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PharmaCompass offers a list of Cefaclor 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 Cefaclor manufacturer or Cefaclor supplier for your needs.
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PharmaCompass also assists you with knowing the Cefaclor API Price utilized in the formulation of products. Cefaclor API Price is not always fixed or binding as the Cefaclor Price is obtained through a variety of data sources. The Cefaclor Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cefaclor manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cefaclor, including repackagers and relabelers. The FDA regulates Cefaclor manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cefaclor 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 Cefaclor supplier is an individual or a company that provides Cefaclor active pharmaceutical ingredient (API) or Cefaclor finished formulations upon request. The Cefaclor suppliers may include Cefaclor API manufacturers, exporters, distributors and traders.
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In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Cefaclor Drug Master File in Korea (Cefaclor KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Cefaclor. The MFDS reviews the Cefaclor KDMF as part of the drug registration process and uses the information provided in the Cefaclor KDMF to evaluate the safety and efficacy of the drug.
After submitting a Cefaclor 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 Cefaclor API can apply through the Korea Drug Master File (KDMF).
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