Monday, October 12, 2020 7:19:39 PM
(2) Information regarding both on- and off-label prescriptions is readily available to the public from publications and databases to which most pharmaceutical companies subscribe,
(3) Pharmacists and other drug dispensing organizations . . . commonly substitute generic drugs for name brand drugs wherever possible — unless specifically instructed otherwise by the physician writing the prescription and in many states, substitution is mandatory
(4) Generic expects to get an "A-B rating" for its drug, which would allow physicians and pharmacists to substitute generic for brand regardless of the indication for which it is to be used, and
(5) Generic should be assumed to have considered the market size and growth potential when it made the strategic decision to file an ANDA and enter the market.
These statements are true ... however precedent holds that mere knowledge of possible infringement by others does not amount to inducement; specific intent and action to induce infringement must be proven. Thus, if a physician, without inducement by Generic, prescribes a use in an infringing manner, Generic's knowledge is legally irrelevant. In the absence of any evidence that Generic has or will promote or encourage doctors to infringe the patent, there has been raised no genuine issue of material fact.
Best,
G
Disclosure: I wrote this post myself, and it expresses my own opinions (IMHO). I am not receiving compensation for it.
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