01 1PT Kimia Farma Sungwun Pharmacopia
01 1Seongun Pharmacopia Co., Ltd.
01 1Povidone iodine
01 1Indonesia
Registrant Name : Seongun Pharmacopia Co., Ltd.
Registration Date : 2025-07-21
Registration Number : 20250721-211-J-1541
Manufacturer Name : PT Kimia Farma Sungwun Pharm...
Manufacturer Address : Delta Silicon 1 – Kawasan Industri Lippo Cikarang, Jl. Angsana Raya Blok A 006 - 01...
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PharmaCompass offers a list of Povidone Iodine 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 Povidone Iodine manufacturer or Povidone Iodine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Povidone Iodine manufacturer or Povidone Iodine supplier.
A POVIDONE IODINE (API) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of POVIDONE IODINE (API), including repackagers and relabelers. The FDA regulates POVIDONE IODINE (API) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. POVIDONE IODINE (API) 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 POVIDONE IODINE (API) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A POVIDONE IODINE (API) supplier is an individual or a company that provides POVIDONE IODINE (API) active pharmaceutical ingredient (API) or POVIDONE IODINE (API) finished formulations upon request. The POVIDONE IODINE (API) suppliers may include POVIDONE IODINE (API) API manufacturers, exporters, distributors and traders.
click here to find a list of POVIDONE IODINE (API) 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 POVIDONE IODINE (API) Drug Master File in Korea (POVIDONE IODINE (API) KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of POVIDONE IODINE (API). The MFDS reviews the POVIDONE IODINE (API) KDMF as part of the drug registration process and uses the information provided in the POVIDONE IODINE (API) KDMF to evaluate the safety and efficacy of the drug.
After submitting a POVIDONE IODINE (API) 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 POVIDONE IODINE (API) API can apply through the Korea Drug Master File (KDMF).
click here to find a list of POVIDONE IODINE (API) suppliers with KDMF on PharmaCompass.
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