01 2AbbVie Ireland NL BV
02 1Abbott Laboratories
03 1Asia Chemical Industries Ltd.
04 1Asia Chemical Industries Ltd. Teva tech site
05 1Bioindustria LIMSpA
06 2Bioindustria LIMSpA_x000D_
07 1Dongbang FTL@Second Pharma Co., Ltd.
08 1Euticals SpA
09 1Hanseochem Co., Ltd.
10 1Hwail Pharmaceutical Co., Ltd.
Registrant Name : Ilyang Pharmaceutical Co., Ltd.
Registration Date : 2013-04-11
Registration Number : 20060707-48-B-224-08(2)
Manufacturer Name : AbbVie Ireland NL BV
Manufacturer Address : Manorhamilton Road, Sligo, Republic of Ireland
A Terazosin Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Terazosin Hydrochloride, including repackagers and relabelers. The FDA regulates Terazosin Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Terazosin Hydrochloride 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 Terazosin Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Terazosin Hydrochloride supplier is an individual or a company that provides Terazosin Hydrochloride active pharmaceutical ingredient (API) or Terazosin Hydrochloride finished formulations upon request. The Terazosin Hydrochloride suppliers may include Terazosin Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Terazosin Hydrochloride 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 Terazosin Hydrochloride Drug Master File in Korea (Terazosin Hydrochloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Terazosin Hydrochloride. The MFDS reviews the Terazosin Hydrochloride KDMF as part of the drug registration process and uses the information provided in the Terazosin Hydrochloride KDMF to evaluate the safety and efficacy of the drug.
After submitting a Terazosin Hydrochloride 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 Terazosin Hydrochloride API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Terazosin Hydrochloride suppliers with KDMF on PharmaCompass.
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