01 1HLB Pep Co., Ltd.
01 1HLB Pep Co., Ltd.
01 1Arginine vasopressin acetate
01 1South Korea
Registrant Name : HLB Pep Co., Ltd.
Registration Date : 2025-11-27
Registration Number : 20251127-210-J-2068
Manufacturer Name : HLB Pep Co., Ltd.
Manufacturer Address : 773 Jeongjungyeon-ro, Osong-eup, Heungdeok-gu, Cheongju-si, Chungcheongbuk-do
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PharmaCompass offers a list of Arginine Vasopressin 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 Arginine Vasopressin manufacturer or Arginine Vasopressin supplier for your needs.
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A Arginine Vasopressin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Arginine Vasopressin, including repackagers and relabelers. The FDA regulates Arginine Vasopressin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Arginine Vasopressin 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 Arginine Vasopressin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Arginine Vasopressin supplier is an individual or a company that provides Arginine Vasopressin active pharmaceutical ingredient (API) or Arginine Vasopressin finished formulations upon request. The Arginine Vasopressin suppliers may include Arginine Vasopressin API manufacturers, exporters, distributors and traders.
click here to find a list of Arginine Vasopressin 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 Arginine Vasopressin Drug Master File in Korea (Arginine Vasopressin KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Arginine Vasopressin. The MFDS reviews the Arginine Vasopressin KDMF as part of the drug registration process and uses the information provided in the Arginine Vasopressin KDMF to evaluate the safety and efficacy of the drug.
After submitting a Arginine Vasopressin 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 Arginine Vasopressin API can apply through the Korea Drug Master File (KDMF).
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