Coral's API range includes Corticosteroids, Antihistamines. Hormones and Antineoplastics.
01 1M/s Coral Drugs Pvt Ltd
02 1SYMBIOTICA SPECIALITY INGREDIENTS SDN. BHD.
01 1Fluocinolone Acetonide
02 1Fluocinolone Acetonide USP
01 13923/25
02 1WC-0009
01 1India
02 1Malaysia
Coral's API range includes Corticosteroids, Antihistamines. Hormones and Antineoplastics.
Date of Issue : 2025-11-20
Valid Till : 2028-11-19
Written Confirmation Number : WC-0009
Address of the Firm : Plot No. 55, 56 & 57, HSIIDC Industrial Estate, Murthal, Sonipat-131 029, Haryan...
Symbiotica delivers high-quality APIs through advanced R&D, GMP-certified manufacturing, & trusted global pharmaceutical partnerships.
Date of Issue : 2025-05-20
Valid Till : 2028-05-22
Written Confirmation Number : 3923/25
Address of the Firm : No. 518, Jalan Waja 4, Taman Industri Waja, 09000 Kulim, Kedah, Malaysia
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A Fluonid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fluonid, including repackagers and relabelers. The FDA regulates Fluonid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fluonid 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 Fluonid manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Fluonid supplier is an individual or a company that provides Fluonid active pharmaceutical ingredient (API) or Fluonid finished formulations upon request. The Fluonid suppliers may include Fluonid API manufacturers, exporters, distributors and traders.
click here to find a list of Fluonid suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Fluonid written confirmation (Fluonid WC) is an official document issued by a regulatory agency to a Fluonid manufacturer, verifying that the manufacturing facility of a Fluonid active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Fluonid APIs or Fluonid finished pharmaceutical products to another nation, regulatory agencies frequently require a Fluonid WC (written confirmation) as part of the regulatory process.
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