01 2M/s. Apitoria Pharma Private Limited
01 2Oxacillin Sodium Monohydrate Ph. Eur.
01 2WC-0121
01 2India
Oxacillin Sodium Monohydrate Ph. Eur.
Date of Issue : 2022-08-02
Valid Till : 2025-07-02
Written Confirmation Number : WC-0121
Address of the Firm : Plot No. 68-70, 73-91, 95, 96, 260, 261, IDA, Pashamylaram (village), Patancheru...
Oxacillin Sodium Monohydrate Ph. Eur.
Date of Issue : 2022-08-02
Valid Till : 2025-07-02
Written Confirmation Number : WC-0121
Address of the Firm : Plot No. 68-70, 73-91, 95, 96, 260, 261, IDA, Pashamylaram (village), Patancheru...
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A O0353 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of O0353, including repackagers and relabelers. The FDA regulates O0353 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. O0353 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 O0353 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A O0353 supplier is an individual or a company that provides O0353 active pharmaceutical ingredient (API) or O0353 finished formulations upon request. The O0353 suppliers may include O0353 API manufacturers, exporters, distributors and traders.
click here to find a list of O0353 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A O0353 written confirmation (O0353 WC) is an official document issued by a regulatory agency to a O0353 manufacturer, verifying that the manufacturing facility of a O0353 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting O0353 APIs or O0353 finished pharmaceutical products to another nation, regulatory agencies frequently require a O0353 WC (written confirmation) as part of the regulatory process.
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