The company obtained its License to Manufacture Oral Solids from the Pharmacists Council of Nigeria, PCN, in a document titled LETTER OF AUTHORITY TO MANUFACTURE on 1st July 2010 with reference number PCN/C/4459/XV/1841. Thereafter, approval from another regulatory body the National Agency for Food and Drug Administration & Control NAFDAC for commencement of production after successful registration of pioneer products (6) was given on 30th March 2011 with reference number ID8521A/I/196. Full operation for production of pharmaceuticals began in July 2011.

FeccoxPharma Ltd engages in a one-product line manufacture of pharmaceuticals, that is, only liquid dosage form basically syrups & suspensions/mixtures. Pharmaceutical raw materials sourced from reliable vendors subject to internal and external analyses of content are employed in production processes under the strictest of hygienic conditions and in compliance with good manufacturing practice, GMP. Standard Operating Procedures (SOP) are adopted for every single operation in the manufacturing industry, for instance from receiving raw material consignment, quarantine, weighing, in-process checks, analytical procedures, mixing, up to packaging etc

Manufacturing of products is the most important activity in any pharmaceutical setting like ours. In this task, the modus operandi for the various products are contained in a Batch Formulation document containing master formulae and other technical information and must be handled by a licenced Production Pharmacist who leads the team of staff in the production department. Errors of manufacture are minimized to the barest minimum in order to achieve quality product consumable by the society. There are no shortcuts in this process; any defect noticed must be reported to the Quality Control Department for decisive action.