Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
01 1M/s. Symbiotec Pharmalab Ltd
02 1M/s Maharshi Pharmachem
01 1Methyl Prednisolone (BP/EP/USP)
02 1Methylprednisolone USP/BP
01 1WC-0162A2
02 1WC-0485
01 2India
Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
Methyl Prednisolone (BP/EP/USP)
Date of Issue : 2022-08-31
Valid Till : 2025-07-02
Written Confirmation Number : WC-0162A2
Address of the Firm : Plot No. 5, 6, 7 & 8 Special Economic Zone, Phase II, Pithampur, Dist: Dhar, MP-...
Date of Issue : 2020-09-25
Valid Till : 2023-09-24
Written Confirmation Number : WC-0485
Address of the Firm : Block No 203, Vaso-Alindra Road, PO Alindra-387510, Tal-Matar Dist. Kheda, Gujar...
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A NEO-MEDROL manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NEO-MEDROL, including repackagers and relabelers. The FDA regulates NEO-MEDROL manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NEO-MEDROL 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 NEO-MEDROL supplier is an individual or a company that provides NEO-MEDROL active pharmaceutical ingredient (API) or NEO-MEDROL finished formulations upon request. The NEO-MEDROL suppliers may include NEO-MEDROL API manufacturers, exporters, distributors and traders.
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A NEO-MEDROL written confirmation (NEO-MEDROL WC) is an official document issued by a regulatory agency to a NEO-MEDROL manufacturer, verifying that the manufacturing facility of a NEO-MEDROL active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting NEO-MEDROL APIs or NEO-MEDROL finished pharmaceutical products to another nation, regulatory agencies frequently require a NEO-MEDROL WC (written confirmation) as part of the regulatory process.
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