The label for a generic drug must include the generic name and the manufacturer's name to provide essential information regarding the medication. The generic name is particularly important because it identifies the chemical compound and ensures consistency across different manufacturers. This information helps health care providers and patients recognize the drug without confusion stemming from brand names, which may vary. Including the manufacturer's name also aids in identifying the source of the medication, which can be critical for issues related to recalls or quality control.
While other information such as dosage and active ingredients might be included on the label, the defining requirements specifically emphasize the generic name and manufacturer's name to ensure clear identification and to fulfill regulatory standards. This labeling practice enhances patient safety by reducing the risk of medication errors and ensuring that patients receive the correct therapeutic agent as intended.