01 1RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA SPA
01 1Ilsung IS Co., Ltd.
01 1Verapamil hydrochloride
01 1U.S.A
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)
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PharmaCompass offers a list of Verapamil Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, 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.
A Verasal manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Verasal, including repackagers and relabelers. The FDA regulates Verasal manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Verasal 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 Verasal manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Verasal supplier is an individual or a company that provides Verasal active pharmaceutical ingredient (API) or Verasal finished formulations upon request. The Verasal suppliers may include Verasal API manufacturers, exporters, distributors and traders.
click here to find a list of Verasal suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Verasal Drug Master File in Korea (Verasal KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Verasal. The MFDS reviews the Verasal KDMF as part of the drug registration process and uses the information provided in the Verasal KDMF to evaluate the safety and efficacy of the drug.
After submitting a Verasal 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 Verasal API can apply through the Korea Drug Master File (KDMF).
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