01 1Changzhou Sunlight Pharmaceutical Co., Ltd.
01 1Daeshin Pharmaceutical Co., Ltd.
01 1Benzocaine
01 1Blank
Registrant Name : Daeshin Pharmaceutical Co., Ltd.
Registration Date : 2025-06-02
Registration Number : 20250602-211-J-1923
Manufacturer Name : Changzhou Sunlight Pharmaceu...
Manufacturer Address : 216 Yunnan West Road, Benniu Town, Xinbei District, Changzhou City, Jiangsu Province ...
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PharmaCompass offers a list of Benzocaine 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 Benzocaine manufacturer or Benzocaine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Benzocaine manufacturer or Benzocaine supplier.
PharmaCompass also assists you with knowing the Benzocaine API Price utilized in the formulation of products. Benzocaine API Price is not always fixed or binding as the Benzocaine Price is obtained through a variety of data sources. The Benzocaine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 06952_FLUKA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 06952_FLUKA, including repackagers and relabelers. The FDA regulates 06952_FLUKA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 06952_FLUKA 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 06952_FLUKA supplier is an individual or a company that provides 06952_FLUKA active pharmaceutical ingredient (API) or 06952_FLUKA finished formulations upon request. The 06952_FLUKA suppliers may include 06952_FLUKA API manufacturers, exporters, distributors and traders.
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In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a 06952_FLUKA Drug Master File in Korea (06952_FLUKA KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of 06952_FLUKA. The MFDS reviews the 06952_FLUKA KDMF as part of the drug registration process and uses the information provided in the 06952_FLUKA KDMF to evaluate the safety and efficacy of the drug.
After submitting a 06952_FLUKA 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 06952_FLUKA API can apply through the Korea Drug Master File (KDMF).
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