Zdrowie i gospodarka · 20/04/2000

Parenteral Multivitamin Products; Drugs for Human Use; Drug Efficacy Study Implementation; Amendment

The Food and Drug Administration (FDA) is amending the conditions for marketing an effective adult parenteral multivitamin drug product that published in the Federal Register of September 17, 1984 (49 FR 36446). The agency is notifying manufacturers of modifications in the adult formulation and certain portions of the labeling for the products.