“branded generic” where he should have said “authorized generic.” This seems to be a common mistake, but I don’t understand why.
For a while I think the terms were virtually synonymous. For example a quote from this paper:
“BRANDED GENERICS” AS A STRATEGY TO LIMIT CANNIBALIZATION OF PHARMACEUTICAL MARKETS David Reiffen US Commodity Futures Trading Commission and Michael R. Ward University of Texas, Arlington May, 2005
Beginning in late 1992, several producers of drugs with soon-to-expire patents introduced, or authorizing the introduction of, generic versions of their important products just prior to patent expiration. We refer to such products as branded generic or authorized generic drugs.
The following from 2005 is similar:
The U.S. Court of Appeals for the District of Columbia Circuit affirmed the district court's granting of summary judgment for the U.S. Food and Drug Administration (FDA) ruling that the Hatch-Waxman amendments do not prohibit the holder of an approved new drug application (NDA) from marketing a "branded generic" version of its drug during the 180-day exclusivity period provided to the first to file an abbreviated new drug application (ANDA) to market a generic drug. Teva Pharmaceutical Industries v. Crawford, Case No. 05-5004 (D.C. Cir. June 3, 2005) (Ginsburg, C. J.).
Subsequently the term "branded generic" started to be used to describe generics marketed by brand name companies (mostly ex-US for prescription drugs) and I agree it now makes sense to make this the exclusive usage.