Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
01 1Cohance Lifesciences Limited
02 1RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA SPA
01 1(주)애거슨바이오
02 1Ilsung IS Co., Ltd.
01 2Verapamil hydrochloride
01 1India
02 1U.S.A
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Registrant Name : (주)애거슨바이오
Registration Date : 2023-08-01
Registration Number : 20230801-209-J-1528
Manufacturer Name : Cohance Lifesciences Limited
Manufacturer Address : RS 50/1, Mukteswarapuram Village, Jaggaiahpeta Mandal, Krishna District-521 175. Andh...
Registrant Name : Ilsung IS Co., Ltd.
Registration Date : 2021-06-22
Registration Number : 20210622-209-J-1032
Manufacturer Name : RECORDATI INDUSTRIA CHIMICA ...
Manufacturer Address : Via Mediana Cisterna, 4 - 04011 APRILIA (LT)
70
PharmaCompass offers a list of Verapamil Hydrochloride 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 Verapamil Hydrochloride manufacturer or Verapamil Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Verapamil Hydrochloride manufacturer or Verapamil Hydrochloride supplier.
PharmaCompass also assists you with knowing the Verapamil Hydrochloride API Price utilized in the formulation of products. Verapamil Hydrochloride API Price is not always fixed or binding as the Verapamil Hydrochloride Price is obtained through a variety of data sources. The Verapamil Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Verelan SR manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Verelan SR, including repackagers and relabelers. The FDA regulates Verelan SR manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Verelan SR 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 Verelan SR supplier is an individual or a company that provides Verelan SR active pharmaceutical ingredient (API) or Verelan SR finished formulations upon request. The Verelan SR suppliers may include Verelan SR API manufacturers, exporters, distributors and traders.
click here to find a list of Verelan SR 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 Verelan SR Drug Master File in Korea (Verelan SR KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Verelan SR. The MFDS reviews the Verelan SR KDMF as part of the drug registration process and uses the information provided in the Verelan SR KDMF to evaluate the safety and efficacy of the drug.
After submitting a Verelan SR 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 Verelan SR API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Verelan SR suppliers with KDMF on PharmaCompass.
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