01 Inist ST Co., Ltd._x000D_ @Quzhou Aifeimu Chemicla Company Ltd. (Manufacturer of Crude Dapoxetine Hydrochloride) (1)
02 Janssen Pharmaceutica N.V. (1)
03 Nosch Labs Pvt. Ltd@[Starting Material]Synergene Active Ingredients Pvt. Ltd. (1)
04 OLON SPA (1)
01 Inist ST Co., Ltd. (1)
02 Korea Menarini Co., Ltd. (2)
03 Leesung International Co., Ltd. (1)
01 Dapoxetine hydrochloride (4)
01 India (1)
02 Italy (1)
03 South Korea (1)
04 U.S.A (1)
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PharmaCompass offers a list of Dapoxetine Hydrochloride 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 Dapoxetine Hydrochloride manufacturer or Dapoxetine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dapoxetine Hydrochloride manufacturer or Dapoxetine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Dapoxetine Hydrochloride API Price utilized in the formulation of products. Dapoxetine Hydrochloride API Price is not always fixed or binding as the Dapoxetine Hydrochloride Price is obtained through a variety of data sources. The Dapoxetine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 129938-20-1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 129938-20-1, including repackagers and relabelers. The FDA regulates 129938-20-1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 129938-20-1 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 129938-20-1 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 129938-20-1 supplier is an individual or a company that provides 129938-20-1 active pharmaceutical ingredient (API) or 129938-20-1 finished formulations upon request. The 129938-20-1 suppliers may include 129938-20-1 API manufacturers, exporters, distributors and traders.
click here to find a list of 129938-20-1 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 129938-20-1 Drug Master File in Korea (129938-20-1 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of 129938-20-1. The MFDS reviews the 129938-20-1 KDMF as part of the drug registration process and uses the information provided in the 129938-20-1 KDMF to evaluate the safety and efficacy of the drug.
After submitting a 129938-20-1 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 129938-20-1 API can apply through the Korea Drug Master File (KDMF).
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We have 4 companies offering 129938-20-1
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