Alchem offers Phytochemical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
01 1Alchem International Private Limited
01 1Daeshin Pharmaceutical Co., Ltd.
01 1Scopolamine Hydrobromide
01 1India
Alchem offers Phytochemical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
Registrant Name : Daeshin Pharmaceutical Co., Ltd.
Registration Date : 2025-04-30
Registration Number : 20250430-211-J-1889
Manufacturer Name : Alchem International P...
Manufacturer Address : 25/2, Main Mathura Road, Village Kaili, Ballabgarh, Faridabad-121 004, Haryana, India
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PharmaCompass offers a list of Scopolamine Hydrobromide 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 Scopolamine Hydrobromide manufacturer or Scopolamine Hydrobromide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Scopolamine Hydrobromide manufacturer or Scopolamine Hydrobromide supplier.
PharmaCompass also assists you with knowing the Scopolamine Hydrobromide API Price utilized in the formulation of products. Scopolamine Hydrobromide API Price is not always fixed or binding as the Scopolamine Hydrobromide Price is obtained through a variety of data sources. The Scopolamine Hydrobromide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A NCGC00024357-07 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NCGC00024357-07, including repackagers and relabelers. The FDA regulates NCGC00024357-07 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NCGC00024357-07 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 NCGC00024357-07 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A NCGC00024357-07 supplier is an individual or a company that provides NCGC00024357-07 active pharmaceutical ingredient (API) or NCGC00024357-07 finished formulations upon request. The NCGC00024357-07 suppliers may include NCGC00024357-07 API manufacturers, exporters, distributors and traders.
click here to find a list of NCGC00024357-07 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 NCGC00024357-07 Drug Master File in Korea (NCGC00024357-07 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of NCGC00024357-07. The MFDS reviews the NCGC00024357-07 KDMF as part of the drug registration process and uses the information provided in the NCGC00024357-07 KDMF to evaluate the safety and efficacy of the drug.
After submitting a NCGC00024357-07 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 NCGC00024357-07 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of NCGC00024357-07 suppliers with KDMF on PharmaCompass.
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