01 Evonik Corporation (1)
02 Moehs Cantabra SL_x000D_ (1)
03 Alembic Pharmaceuticals Limited (1)
04 Asia Chemical Industries Ltd. (1)
05 Dasan Pharmaceutical Co., Ltd. @[Manufacturer of starting material 'duloxetine hydrochloride'] SCI Pharmtech, Inc. (1)
06 Hanseochem Co., Ltd. (1)
07 Hetero Drugs Limited (2)
08 Hetero Drugs Limited. (1)
09 Ildong Pharmaceutical Co., Ltd. (1)
10 Inist ST Co., Ltd. (1)
11 Korea Biochem Pharmaceutical Co., Ltd. (1)
12 Kyungbo Pharmaceutical Co., Ltd. (1)
13 Lilly del Caribe, Inc. (1)
14 MSN Laboratories PVT LTD (1)
15 Macleods Pharmaceuticals Limited (2)
16 Nosch Labs Pvt. Ltd@[Manufacturer of starting material (duloxetine hydrochloride)] Nosch Labs Pvt. Ltd (4)
17 Nosch Labs private limited Unit-II (1)
18 SCI Pharmtech, Inc. (1)
19 Shodhana Laboratories Limited (1)
20 Titan Laboratories Pvt. Ltd. (2)
21 Union Quimico Farmaceutica, SA (1)
22 [Starting material (duloxetine hydrochloride) manufacturer] Nosch Labs Pvt. Ltd@Nosch Labs Pvt. Ltd (1)
01 Aging Life Science Co., Ltd. (1)
02 Dasan Pharmaceutical Co., Ltd. (1)
03 Hanseochem Co., Ltd. (1)
04 Hwanin Pharmaceutical Co., Ltd. (1)
05 Iksoo Pharmaceutical Co., Ltd. (1)
06 Ildong Pharmaceutical Co., Ltd. (1)
07 Inist ST Co., Ltd. (1)
08 Kookjeon Pharmaceutical Co., Ltd. (1)
09 Korea Biochem Pharmaceutical Co., Ltd. (1)
10 Korea Lily Co., Ltd. (2)
11 Korea Pharmaceutical Co., Ltd. (2)
12 Kyungbo Pharmaceutical Co., Ltd. (1)
13 Myungin Pharmaceutical Co., Ltd. (2)
14 Pharmapia Co., Ltd. (2)
15 Saehan Pharmaceutical Co., Ltd. (1)
16 Samo Pharmaceutical Co., Ltd. (1)
17 Sandoz Korea Co., Ltd. (1)
18 Sangjin Trading Co., Ltd. (1)
19 Sungjin Exim Co., Ltd. (1)
20 UNUST Co., Ltd. (1)
21 Unimed Pharmaceutical Co., Ltd. (1)
22 Wonpoong Pharmaceutical Co., Ltd. (3)
01 Duloxetine hydrochloride (2)
02 duloxetine hydrochloride (26)
01 Germany (1)
02 India (16)
03 Israel (1)
04 South Korea (6)
05 Spain (2)
06 Taiwan (1)
07 U.S.A (1)
48
PharmaCompass offers a list of Duloxetine 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 Duloxetine manufacturer or Duloxetine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Duloxetine manufacturer or Duloxetine supplier.
PharmaCompass also assists you with knowing the Duloxetine API Price utilized in the formulation of products. Duloxetine API Price is not always fixed or binding as the Duloxetine Price is obtained through a variety of data sources. The Duloxetine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cymbalta manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cymbalta, including repackagers and relabelers. The FDA regulates Cymbalta manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cymbalta 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 Cymbalta manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cymbalta supplier is an individual or a company that provides Cymbalta active pharmaceutical ingredient (API) or Cymbalta finished formulations upon request. The Cymbalta suppliers may include Cymbalta API manufacturers, exporters, distributors and traders.
click here to find a list of Cymbalta 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 Cymbalta Drug Master File in Korea (Cymbalta KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Cymbalta. The MFDS reviews the Cymbalta KDMF as part of the drug registration process and uses the information provided in the Cymbalta KDMF to evaluate the safety and efficacy of the drug.
After submitting a Cymbalta 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 Cymbalta API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Cymbalta suppliers with KDMF on PharmaCompass.
We have 19 companies offering Cymbalta
Get in contact with the supplier of your choice: