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Annual · values202520242023202220212020201920182017201620152014
Operating Cash Flow827.99 M USD572.84 M USD159.26 M USD175.90 M USD304.54 M USD85.36 M USD48.26 M USD20.21 M USD-8.76 M USD-227.84 M USD-221.69 M USD-73.54 M USD
Depreciation & Amortization79.56 M USD96.43 M USD104.39 M USD101.97 M USD108.04 M USD105.17 M USD105.30 M USD95.67 M USD87.86 M USD96.91 M USD47.19 M USD45.87 M USD
Stock-Based Compensation181.41 M USD201.57 M USD207.10 M USD196.31 M USD197.26 M USD189.71 M USD159.87 M USD148.82 M USD140.26 M USD134.64 M USD111.53 M USD88.23 M USD
Capital Expenditures103.04 M USD85.42 M USD96.69 M USD120.96 M USD95.58 M USD114.31 M USD145.03 M USD144.62 M USD199.22 M USD148.38 M USD227.65 M USD118.83 M USD
Cash Flow from Investing-414.24 M USD136.49 M USD-111.24 M USD-20.03 M USD-366.31 M USD-53.62 M USD-31.03 M USD264.35 M USD-305.46 M USD-484.05 M USD-1.18 B USD194.56 M USD
Cash Flow from Financing-42.39 M USD-526.45 M USD-18.73 M USD-18.65 M USD-48000 USD181.12 M USD-74.67 M USD-388.01 M USD507.14 M USD727.11 M USD927.91 M USD185.69 M USD
Dividends Paid
Stock Buybacks0 USD0 USD50.00 M USD0 USD0 USD
Free Cash Flow724.96 M USD487.42 M USD62.57 M USD54.94 M USD208.96 M USD-28.95 M USD-96.76 M USD-124.41 M USD-207.98 M USD-376.22 M USD-449.34 M USD-192.37 M USD

BioMarin Pharmaceutical Inc. is a leading global biotechnology company specializing in the development and commercialization of therapies for people with serious and life-threatening rare genetic diseases. Its portfolio includes eight approved treatments targeting conditions such as mucopolysaccharidosis types I, IVA, and VI (branded as Aldurazyme, Vimizim, and Naglazyme), phenylketonuria (Kuvan), achondroplasia (Voxzogo), Batten disease (Brineura), Lambert-Eaton myasthenic syndrome (Firdapse), and hemophilia A (Roctavian). These therapies encompass enzyme replacement therapies, gene therapies, and small molecule drugs designed to address the underlying genetic causes of these disorders. BioMarin Pharmaceutical Inc. operates in more than 70 countries across the United States, Europe, Latin America, the Middle East, and Asia Pacific, serving patient communities through innovative genetic science and molecular biology expertise. Founded in 1997 and headquartered in San Rafael, California, the company maintains a robust pipeline of clinical and preclinical candidates focused on skeletal dysplasias, liver diseases, and muscular dystrophies, reinforcing its pivotal role in the rare disease biotechnology sector.