01 1Swati Spentose Private Limited (Unit-Ⅱ)
01 1Sanil Pharma Co., Ltd.
01 1Fluocinolone acetonide
01 1India
Registrant Name : Sanil Pharma Co., Ltd.
Registration Date : 2025-06-05
Registration Number : 20250605-211-J-1898
Manufacturer Name : Swati Spentose Private Limit...
Manufacturer Address : Plot No. A-1/2110-2111, III Phase, GIDC VAPI, City: Vapi - 396 195, Dist. Valsad, Guj...
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PharmaCompass offers a list of Fluocinolone Acetonide 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 Fluocinolone Acetonide manufacturer or Fluocinolone Acetonide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Fluocinolone Acetonide manufacturer or Fluocinolone Acetonide supplier.
PharmaCompass also assists you with knowing the Fluocinolone Acetonide API Price utilized in the formulation of products. Fluocinolone Acetonide API Price is not always fixed or binding as the Fluocinolone Acetonide Price is obtained through a variety of data sources. The Fluocinolone Acetonide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dermalar manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dermalar, including repackagers and relabelers. The FDA regulates Dermalar manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dermalar 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 Dermalar manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dermalar supplier is an individual or a company that provides Dermalar active pharmaceutical ingredient (API) or Dermalar finished formulations upon request. The Dermalar suppliers may include Dermalar API manufacturers, exporters, distributors and traders.
click here to find a list of Dermalar 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 Dermalar Drug Master File in Korea (Dermalar KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Dermalar. The MFDS reviews the Dermalar KDMF as part of the drug registration process and uses the information provided in the Dermalar KDMF to evaluate the safety and efficacy of the drug.
After submitting a Dermalar 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 Dermalar API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Dermalar suppliers with KDMF on PharmaCompass.
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