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 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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A component of Neo-Synalar written confirmation (component of Neo-Synalar WC) is an official document issued by a regulatory agency to a component of Neo-Synalar manufacturer, verifying that the manufacturing facility of a component of Neo-Synalar active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting component of Neo-Synalar APIs or component of Neo-Synalar finished pharmaceutical products to another nation, regulatory agencies frequently require a component of Neo-Synalar WC (written confirmation) as part of the regulatory process.
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