The group of hepatobiliary contrast agents comprises two gadolinium-based contrast agents (GBCAs) that show a specific amount of hepatocellular uptake and biliary excretion. Gadobenate dimeglumine (Gd-BOPTA; Bracco Diagnostics) and gadoxetic acid (Gd-EOB-DTPA; Bayer Healthcare) are US Food and Drug Administration (FDA)-approved agents for magnetic resonance imaging (MRI) and for detection and characterization of liver lesions, respectively. A third agent with hepatobiliary properties, gadofosveset trisodium, has recently been discontinued.The success of these so-called hepatobiliary contrast agents (hbGBCAs) is essentially related to satisfying the fundamental motive in MRI-that is, the pursuit to structurally characterize tissues or lesions. Specifically, MRI's high intrinsic soft tissue contrast with its ability to enhance specific tissue characteristics is further amended by the ability of hbGBCAs to detect hepatocytes and biliary canaliculi. In combination, the use of hbGBCAs in MRI is a powerful diagnostic instrument.hbGBCAs carry the dual properties of acting like ''conventional'' GBCAs during the first pass and early phases of contrast enhancement, and by revealing the characteristic delayed or hepatobiliary enhancement. In the initial phases after injection, their contrast enhancement is dominated by the distribution in vessels and the extracellular space like in conventional GBCAs. However, unlike other GBCAs, hbGBCAs are then taken up by functional hepatocytes. As a result, there is a persistent enhancement in hepatocytes that allows for identifying lesions of Abbreviations: EMA, European Medicines Agency; FDA, US Food and Drug Administration; FNH, focal nodular hyperplasia; GBCA, gadolinium-based contrast agent; HA, hepatic adenoma; hbGBCA, hepatobiliary GBCA; MRC, magnetic resonance cholangiography; MRCP, magnetic resonance cholangiopancreatography; MRI, magnetic resonance imaging; NSF, nephrogenic systemic fibrosis.From the *University of L€ ubeck, Campus L€ ubeck, and