Apex Healthcare Limited: ISO 9001:2008, WHO-GMP, US FDA-audited manufacturer & exporter of APIs, bulk drugs, and formulations.
01 1M/s Apex Healthcare limited
02 1M/s Nosch Labs Pvt ltd
03 1M/s. Global Calcium Private Ltd
04 1M/sGlobal Calcium Pvt Ltd
01 1Phenyramidol Hydrochloride IH
02 1Phenyramidol Hydrochloride IHS
03 2Phenyramidol Hydrochloride IP
01 1WC--0104
02 1WC-0104
03 1WC-0384
04 1WC-0409
01 4India
Apex Healthcare Limited: ISO 9001:2008, WHO-GMP, US FDA-audited manufacturer & exporter of APIs, bulk drugs, and formulations.
Date of Issue : 2024-03-01
Valid Till : 2026-12-31
Written Confirmation Number : WC-0409
Address of the Firm : 4710, 4711, 4707-A/8, 4707-A/9, GIDC, Industrial Estate, Ankleshwar, Dist.Bharuc...
Date of Issue : 2025-07-22
Valid Till : 2028-07-07
Written Confirmation Number : WC--0104
Address of the Firm : 124, 125 and 126, SIPCOT Industrial Complex, Hosur -635126, Tamil Nadu, India
Date of Issue : 2022-06-17
Valid Till : 2025-07-07
Written Confirmation Number : WC-0104
Address of the Firm : 125 & 126, Sipcot Industrial Complex, Hosur 635126, Tamil Nadu
Phenyramidol Hydrochloride IHS
Date of Issue : 2022-12-30
Valid Till : 2026-01-05
Written Confirmation Number : WC-0384
Address of the Firm : UNIT-IV, Sy No. 332, 333 & 335 Veliminedu (Village), Chityal (Mandal), Nalgonda ...
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A C13H14N2O manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of C13H14N2O, including repackagers and relabelers. The FDA regulates C13H14N2O manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. C13H14N2O 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 C13H14N2O supplier is an individual or a company that provides C13H14N2O active pharmaceutical ingredient (API) or C13H14N2O finished formulations upon request. The C13H14N2O suppliers may include C13H14N2O API manufacturers, exporters, distributors and traders.
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A C13H14N2O written confirmation (C13H14N2O WC) is an official document issued by a regulatory agency to a C13H14N2O manufacturer, verifying that the manufacturing facility of a C13H14N2O active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting C13H14N2O APIs or C13H14N2O finished pharmaceutical products to another nation, regulatory agencies frequently require a C13H14N2O WC (written confirmation) as part of the regulatory process.
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