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 Dishman Carbogen Amcis Limited
03 1M/sKreative Organics Private limited
01 1Bisacodyl BP/EP/USP
02 1Bisacodyl BP/USP/EP
03 1Bisacodyl BP/USP/Ph. Eur
01 1WC-0136n
02 1WC-0180
03 1WC-0409
01 3India
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 : 2022-09-16
Valid Till : 2025-02-07
Written Confirmation Number : WC-0136n
Address of the Firm : 1216/11,12,1216/20 to 26, G.I.D.C Estate Phase IV,Naroda, Dist -Ahmedabad-382330...
Date of Issue : 2022-08-29
Valid Till : 2025-07-26
Written Confirmation Number : WC-0180
Address of the Firm : D-123, Phase -III, IDA., Jeedimetla (V), Quthbullapur (M), Medchal-Malkajgiri Di...
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A LS-2218 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LS-2218, including repackagers and relabelers. The FDA regulates LS-2218 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LS-2218 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 LS-2218 supplier is an individual or a company that provides LS-2218 active pharmaceutical ingredient (API) or LS-2218 finished formulations upon request. The LS-2218 suppliers may include LS-2218 API manufacturers, exporters, distributors and traders.
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A LS-2218 written confirmation (LS-2218 WC) is an official document issued by a regulatory agency to a LS-2218 manufacturer, verifying that the manufacturing facility of a LS-2218 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting LS-2218 APIs or LS-2218 finished pharmaceutical products to another nation, regulatory agencies frequently require a LS-2218 WC (written confirmation) as part of the regulatory process.
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