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.
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A component of Neo-Synalar manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of component of Neo-Synalar, including repackagers and relabelers. The FDA regulates component of Neo-Synalar manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. component of Neo-Synalar API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A component of Neo-Synalar supplier is an individual or a company that provides component of Neo-Synalar active pharmaceutical ingredient (API) or component of Neo-Synalar finished formulations upon request. The component of Neo-Synalar suppliers may include component of Neo-Synalar API manufacturers, exporters, distributors and traders.
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In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a component of Neo-Synalar Drug Master File in Korea (component of Neo-Synalar KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of component of Neo-Synalar. The MFDS reviews the component of Neo-Synalar KDMF as part of the drug registration process and uses the information provided in the component of Neo-Synalar KDMF to evaluate the safety and efficacy of the drug.
After submitting a component of Neo-Synalar 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 component of Neo-Synalar API can apply through the Korea Drug Master File (KDMF).
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