Apex Healthcare: ISO 9001:2008, WHO-GMP, US FDA-approved manufacturer & exporter of APIs, bulk drugs, and formulations.
01 1M/s. Apex Healthcare Limited
02 1M/s. Dishman Pharmaceuticals and Chemicals Ltd.
03 1M/s. Kreative Organics Pvt. Ltd.
01 1Sodium Pico Sulfate (BP/Ph. Eur.)
02 1Sodium Picosulfate (BP/JP/EP)
03 1Sodium Picosulphate BP/EP/USP
01 1WC-0136n
02 1WC-0180
03 1WC-0409
01 3India
Apex Healthcare: ISO 9001:2008, WHO-GMP, US FDA-approved 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 : 2025-07-22
Written Confirmation Number : WC-0136n
Address of the Firm : 1216/11, 12, 1216/20 to 26, GIDC Estate, Phase-IV, Naroda, Dist. Ahmedabad- 382 ...
Sodium Pico Sulfate (BP/Ph. Eur.)
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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PharmaCompass offers a list of Sodium Picosulfate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Sodium Picosulfate manufacturer or Sodium Picosulfate supplier for your needs.
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A Laxoberon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Laxoberon, including repackagers and relabelers. The FDA regulates Laxoberon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Laxoberon 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 Laxoberon supplier is an individual or a company that provides Laxoberon active pharmaceutical ingredient (API) or Laxoberon finished formulations upon request. The Laxoberon suppliers may include Laxoberon API manufacturers, exporters, distributors and traders.
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A Laxoberon written confirmation (Laxoberon WC) is an official document issued by a regulatory agency to a Laxoberon manufacturer, verifying that the manufacturing facility of a Laxoberon active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Laxoberon APIs or Laxoberon finished pharmaceutical products to another nation, regulatory agencies frequently require a Laxoberon WC (written confirmation) as part of the regulatory process.
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