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Two methods were described for the simultaneous determination of ciprofloxacin HCl (CIP) and moxifloxacin HCl (MOX) in their binary mixture present in industrial wastewater. A solid-phase extraction procedure (SPE) based on retention on HLB OASIS cartridges and elution with a mixture of methanol-water in acidic medium was preformed, and then both fluoroquinolones were separated using two chromatographic methods. The first method was based on high-performance liquid chromatographic separation of the two drugs on reversed-phase Zorbax C18 column. The mobile phase consisted of monobasic potassium phosphate (50 mM, pH 2.5, adjusted with phosphoric acid) and acetonitrile (80:20, v/v). Flow rate was 1 mL min(-1). Quantitation was achieved with ultraviolet (UV) detection at 278 nm. Linearity was found to be over the concentration range of 1-50 mu g mL(-1) for both CIP and MOX. The second method was based on the thin-layer chromatographic (TLC) separation of the two drugs followed by densitometric measurements of their bands at 278 nm. The separation was carried out on silica gel 60 F-254 plates, using methanol, ammonia, and methylene chloride (55:35:20, v/v) as a developing system. The linearity was found to be in the range of 0.25-2.5 mu g band(-1) for both CIP and MOX. Both methods were optimized and validated as per International Conference on Harmonization (ICH) guidelines. Separation was developed on spiked water samples and checked on process wastewaters of industrial origin after SPE sample pretreatment.