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Zdrowie i gospodarka · 18/07/2003

New Animal Drugs; Laidlomycin

The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect approval of a supplemental new animal drug application (NADA) filed by Alpharma Inc. The supplemental NADA provides for the establishment of a tolerance for residues of laidlomycin in cattle liver. The previously established acceptable daily intake (ADI) for total residues of laidlomycin is also being codified.

Source: Federal Register — Food and Drug AdministrationOpen original release →