ABOUT US

ABOUT US

GENERAL INFORMATION

Brief Information

FeccoxPharma& Gen. Ent. Ltd is one of the indigenous pharmaceutical companies in the ancient city of Kano. It was incorporated as limited liabilities (by shares) company on 21st October 1994 under the COMPANIES AND ALLIED MATTERS ACT 1990 with RC no 255883. The premise is located in an industrial site at no 2 Jabba layout off airport road enroots to Kano Free Trade Zone Complex. The company is being managed by a Board of Directors. However, the day-to-day running of the firm is handled by the Managing Director Mr Williams Mbah ably supported by vibrant workforce of technical and skilled employees.

The company engages in the pharmaceutical manufacture of only syrups and suspension at present but with a view to adding solid dosage form in the near future.

Vision

Feccox Pharmaceuticals envisioned becoming world class pharmaceutical products producers that is passionate about the quality of its products and life of the general populace.

This company is committed to procure, produce and supply medicines and health products of assured quality. In order to achieve this objective, the company has set up a Quality Assurance Policy.

Motto

Adding Value to life

Pharmaceutical Manufacturing Operation

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.