Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1Moehs Cantabra SL
02 2Aarti Pharmalabs limited Unit-IV
03 1Siegfried Ltd
04 1Solara Active Pharma Sciences Limited
05 1Standard Chem.&Pharm. Co., Ltd.@[Venlafaxine Hydrochloride Manufacturing Plant]Aarti Industries Limited
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Registrant Name : Samoh Pharmaceutical Co., Ltd.
Registration Date : 2021-04-16
Registration Number : 20210416-209-J-811
Manufacturer Name : Moehs Cantabra SL
Manufacturer Address : Poligono Industrial Requejada, Polanco 39313, Cantabria, Spain
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Registrant Name : Myungin Pharmaceutical Co., Ltd.
Registration Date : 2019-01-07
Registration Number : 20181113-209-J-273(1)
Manufacturer Name : Aarti Pharmalabs limited Uni...
Manufacturer Address : Plot No. E-50, 50/1 & 59/1, MIDC, Tarapur, Taluka & District-Palghar 401506 Maharasht...
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Registrant Name : Lee Sung International Co., Ltd.
Registration Date : 2018-11-13
Registration Number : 20181113-209-J-273
Manufacturer Name : Aarti Pharmalabs limited Uni...
Manufacturer Address : Plot No. E-50, 50/1 & 59/1, MIDC, Tarapur, Taluka & District-Palghar 401506 Maharasht...
A Venlafaxine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Venlafaxine Hydrochloride, including repackagers and relabelers. The FDA regulates Venlafaxine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Venlafaxine 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 Venlafaxine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Venlafaxine Hydrochloride supplier is an individual or a company that provides Venlafaxine Hydrochloride active pharmaceutical ingredient (API) or Venlafaxine Hydrochloride finished formulations upon request. The Venlafaxine Hydrochloride suppliers may include Venlafaxine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Venlafaxine 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 Venlafaxine Hydrochloride Drug Master File in Korea (Venlafaxine Hydrochloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Venlafaxine Hydrochloride. The MFDS reviews the Venlafaxine Hydrochloride KDMF as part of the drug registration process and uses the information provided in the Venlafaxine Hydrochloride KDMF to evaluate the safety and efficacy of the drug.
After submitting a Venlafaxine 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 Venlafaxine Hydrochloride API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Venlafaxine Hydrochloride suppliers with KDMF on PharmaCompass.
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