FDA now accepts electronic listings on a voluntary basis

摘要

It must know the specific quantity of each active ingredient in order to ensure that an NDC number fits different product strengths Similarly, FDA wants data on a drug's dosage form to distinguish tablets from, say, capsules. A box with 12 unit-of-use blisters would have a different code from each individual blister, a distinction that could enhance the accuracy and value of bar codes and, thus, reduce medication errors Patients with allergies must know about excipi-ents And, information on tablet imprints would help FDA investigate reports of counterfeiting and adverse events.