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 1Sodium Picosulfate BP/EP/USP
02 1Sodium Picosulfate BP/JP
03 1Sodium Picosulfate BP/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 Laxoberal manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Laxoberal, including repackagers and relabelers. The FDA regulates Laxoberal manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Laxoberal 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 Laxoberal supplier is an individual or a company that provides Laxoberal active pharmaceutical ingredient (API) or Laxoberal finished formulations upon request. The Laxoberal suppliers may include Laxoberal API manufacturers, exporters, distributors and traders.
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A Laxoberal written confirmation (Laxoberal WC) is an official document issued by a regulatory agency to a Laxoberal manufacturer, verifying that the manufacturing facility of a Laxoberal active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Laxoberal APIs or Laxoberal finished pharmaceutical products to another nation, regulatory agencies frequently require a Laxoberal WC (written confirmation) as part of the regulatory process.
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