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