(410 ILCS 620/2.25) (from Ch. 56 1/2, par. 502.25)
Sec. 2.25.
"New animal drug" means any drug intended for use
for animals other than man, including any drug intended for use in animal
feed but not including such animal feed (1) the composition of which is
such that such drug is not generally recognized, among experts qualified
by scientific training and experience to evaluate the safety and effectiveness
of animal drugs, as safe and effective for use under the condition prescribed,
recommended or suggested in the labeling thereof; except that such a drug
not so recognized shall not be deemed to be a "new animal drug" if at any
time prior to June 25, 1938, it was subject to the Food and Drug Act of
June 30, 1906, as amended, and if at such time its labeling contained the
same representations concerning the conditions of its use; or (2) the composition
of which is such that such drug, as a result of investigations to determine
its safety and effectiveness for use under such conditions, has become so
recognized but which has not, other than in such investigations, been
used to a material extent or for a material time under such conditions;
or (3) which drug is composed wholly or partly of any kind of penicillin,
streptomycin, chlortetracycline, chloramphenicol or bacitracin, or any
derivative thereof, except when there is in effect a published order of
the Secretary of Health and Human Services declaring such drug not to be
a new animal drug on the grounds that the requirement of certification
of batches of such drug, as provided for in Section 512(n) of the Federal
Act, is not necessary to insure that the objectives specified in paragraph
(3) thereof are achieved and that neither paragraph (1) nor (2) above applies
to such drug.
(Source: P.A. 84-891.)
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