Alchem offers Botanical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
01 2Alchem International Private Limited
02 1Australian Alkaloids Pty Ltd
01 1Daeshin Muyak Co., Ltd.
02 1Myeongmun Bio Co., Ltd.
03 1Pharmapia Co., Ltd.
01 3Scopolamine hydrobromide hydrate
01 1Australia
02 2India
Alchem offers Botanical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
Scopolamine hydrobromide hydrate
Registrant Name : Pharmapia Co., Ltd.
Registration Date : 2026-04-03
Registration Number : 20250430-211-J-1889(1)
Manufacturer Name : Alchem International P...
Manufacturer Address : 25/2, Main Mathura Road, Village Kaili, Ballabgarh, Faridabad-121 004, Haryana, India
Alchem offers Botanical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
Scopolamine hydrobromide hydrate
Registrant Name : Daeshin Muyak 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
Scopolamine hydrobromide hydrate
Registrant Name : Myeongmun Bio Co., Ltd.
Registration Date : 2025-07-01
Registration Number : 20250701-211-J-1950
Manufacturer Name : Australian Alkaloids Pty Ltd
Manufacturer Address : Oilseeds Road Memerambi (Via Kingaroy) QLD 4610, Australia
80
PharmaCompass offers a list of Scopolamine Hydrobromide 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 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.
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, and COA 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, 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 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.
We have 2 companies offering NCGC00024357-07
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