Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

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01 4Granules India Limited
02 1Zhejiang Haizhou Pharmaceutical Co., Ltd.
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01 1Daeshin Pharmaceutical Co., Ltd.
02 1Hwail Pharmaceutical Co., Ltd.
03 1IMCD Korea Co., Ltd.
04 1Insung Trading Co., Ltd.
05 1Masung LS Co., Ltd.
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01 5Guaifenesin
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01 1China
02 4India
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
Registrant Name : Hwail Pharmaceutical Co., Ltd.
Registration Date : 2021-11-30
Registration Number : 20210309-211-J-857(3)
Manufacturer Name : Granules India Limited
Manufacturer Address : 15A/1, IDA, Phase-III, Jeedimetla, Quthbullapur Mandal, Malkajgiri Dist – 500055, T...
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
Registrant Name : Insung Trading Co., Ltd.
Registration Date : 2021-03-09
Registration Number : 20210309-211-J-857
Manufacturer Name : Granules India Limited
Manufacturer Address : 15A/1, IDA, Phase-III, Jeedimetla, Quthbullapur Mandal, Malkajgiri Dist – 500055, T...
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
Registrant Name : Daeshin Pharmaceutical Co., Ltd.
Registration Date : 2021-07-05
Registration Number : 20210309-211-J-857(2)
Manufacturer Name : Granules India Limited
Manufacturer Address : 15A/1, IDA, Phase-III, Jeedimetla, Quthbullapur Mandal, Malkajgiri Dist – 500055, T...
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
Registrant Name : IMCD Korea Co., Ltd.
Registration Date : 2021-06-04
Registration Number : 20210309-211-J-857(1)
Manufacturer Name : Granules India Limited
Manufacturer Address : 15A/1, IDA, Phase-III, Jeedimetla, Quthbullapur Mandal, Malkajgiri Dist-500 055.,Tela...
Registrant Name : Masung LS Co., Ltd.
Registration Date : 2025-10-10
Registration Number : 20251010-211-J-2307
Manufacturer Name : Zhejiang Haizhou Pharmaceuti...
Manufacturer Address : Yanhai Industrial Zone, Linhai City, Zhejiang 317016, China

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PharmaCompass offers a list of Guaifenesin 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 Guaifenesin manufacturer or Guaifenesin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Guaifenesin manufacturer or Guaifenesin supplier.
PharmaCompass also assists you with knowing the Guaifenesin API Price utilized in the formulation of products. Guaifenesin API Price is not always fixed or binding as the Guaifenesin Price is obtained through a variety of data sources. The Guaifenesin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Aresol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aresol, including repackagers and relabelers. The FDA regulates Aresol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aresol 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 Aresol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Aresol supplier is an individual or a company that provides Aresol active pharmaceutical ingredient (API) or Aresol finished formulations upon request. The Aresol suppliers may include Aresol API manufacturers, exporters, distributors and traders.
click here to find a list of Aresol 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 Aresol Drug Master File in Korea (Aresol KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Aresol. The MFDS reviews the Aresol KDMF as part of the drug registration process and uses the information provided in the Aresol KDMF to evaluate the safety and efficacy of the drug.
After submitting a Aresol 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 Aresol API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Aresol suppliers with KDMF on PharmaCompass.
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