Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
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 : 아이엠씨디코리아주식회사
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...
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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 Nasatab LA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nasatab LA, including repackagers and relabelers. The FDA regulates Nasatab LA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nasatab LA 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 Nasatab LA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nasatab LA supplier is an individual or a company that provides Nasatab LA active pharmaceutical ingredient (API) or Nasatab LA finished formulations upon request. The Nasatab LA suppliers may include Nasatab LA API manufacturers, exporters, distributors and traders.
click here to find a list of Nasatab LA 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 Nasatab LA Drug Master File in Korea (Nasatab LA KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Nasatab LA. The MFDS reviews the Nasatab LA KDMF as part of the drug registration process and uses the information provided in the Nasatab LA KDMF to evaluate the safety and efficacy of the drug.
After submitting a Nasatab LA 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 Nasatab LA API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Nasatab LA suppliers with KDMF on PharmaCompass.
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