01 1M/s Symed Labs Limited
02 1M/s. Tyche Industries Limited
01 1Racecadotril Ph. Eur
02 1Racecardotril Ph.Eur.
01 1WC-0072
02 1WC-0231
01 2India
Date of Issue : 2025-09-29
Valid Till : 2028-08-09
Written Confirmation Number : WC-0072
Address of the Firm : Unit-II, Plot No.: 25/B, Phase -III, Jeedimetla(V),Quthbullapur (M), Medchal -Ma...
Date of Issue : 2025-08-01
Valid Till : 2028-07-02
Written Confirmation Number : WC-0231
Address of the Firm : D. No 6-233, Sarpavaram, Kakinada -533005, Kakinada District, Andhra Pradesh, In...
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A REDOTIL manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of REDOTIL, including repackagers and relabelers. The FDA regulates REDOTIL manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. REDOTIL 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 REDOTIL manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A REDOTIL supplier is an individual or a company that provides REDOTIL active pharmaceutical ingredient (API) or REDOTIL finished formulations upon request. The REDOTIL suppliers may include REDOTIL API manufacturers, exporters, distributors and traders.
click here to find a list of REDOTIL suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A REDOTIL written confirmation (REDOTIL WC) is an official document issued by a regulatory agency to a REDOTIL manufacturer, verifying that the manufacturing facility of a REDOTIL active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting REDOTIL APIs or REDOTIL finished pharmaceutical products to another nation, regulatory agencies frequently require a REDOTIL WC (written confirmation) as part of the regulatory process.
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