1880
LAWS OF MARYLAND
Ch. 240
(6) IT HAS BEEN FOUND UNDER THE FEDERAL ACT OR
BY THE SECRETARY TO BE A DRUG LIABLE TO DETERIORATION, AND:
(I) IT IS NOT PACKAGED IN THE FORM AND
MANNER REQUIRED BY THE RULES AND REGULATIONS ADOPTED UNDER
THE FEDERAL ACT OR BY THE SECRETARY; OR
(II) ITS LABEL DOES NOT BEAR A STATEMENT
OF PRECAUTIONS AS REQUIRED BY THOSE RULES AND REGULATIONS;
(7) IT IS A PRESCRIPTION DRUG THAT WAS
MANUFACTURED AFTER JULY 1, 1976 AND ITS LABEL DOES NOT BEAR
THE NAME OF THE ACTUAL MANUFACTURER OF THE DRUG;
(8) ITS CONTAINER IS MADE, FORMED, OR FILLED IN
A MANNER THAT IS MISLEADING;
(9) IT IS AN IMITATION OF ANOTHER DRUG;
(10) IT IS OFFERED FOR SALE UNDER THE NAME OF
ANOTHER DRUG;
(11) IT IS OR IT IS PURPORTED TO BE A DRUG THAT
IS COMPOSED IN WHOLE OR IN PART OF INSULIN AND IT IS NOT
FROM A BATCH FOR WHICH A CURRENTLY UNEXPIRED CERTIFICATE OR
RELEASE HAS BEEN ISSUED UNDER THE FEDERAL ACT;
(12) IT IS OR IT IS PURPORTED TO BE A DRUG
COMPOSED IN WHOLE OR IN PART OF ANY KIND OF PENICILLIN,
STREPTOMYCIN, CHLORTETRACYCLINE, CHLORAMPHENICOL,
BACITRACIN, OR ANY OTHER ANTIBIOTIC DRUG, OR OF ANY
DERIVATIVE OF THESE DRUGS AND, UNLESS THE DRUG HAS BEEN
EXEMPTED BY RULES AND REGULATIONS ADOPTED UNDER THE FEDERAL
ACT, IT IS NOT FROM A BATCH FOR WHICH A CURRENTLY UNEXPIRED
CERTIFICATE OR RELEASE HAS BEEN ISSUED UNDER THE FEDERAL
ACT;
(13) IT IS A COLOR ADDITIVE THAT IS INTENDED TO
BE USED IN OR ON A DRUG FOR THE PURPOSE OF COLORING ONLY AND
ITS PACKAGING OR LABELING DOES NOT CONFORM TO ANY
REQUIREMENT ADOPTED UNDER § 4-239 OF THIS SUBTITLE; OR
(14) IT IS A PRESCRIPTION DRUG THAT IS
DISTRIBUTED OR OFFERED FOR SALE IN THIS STATE, AND THE
MANUFACTURER, PACKER, OR DISTRIBUTOR OF THE DRUG DOES NOT
INCLUDE IN ANY ADVERTISEMENT, OR IN ANY OTHER DESCRIPTIVE
PRINTED MATTER THAT IT ISSUES OR CAUSES TO BE ISSUED
REGARDING THE DRUG, A TRUE STATEMENT OF:
(I) THE ESTABLISHED NAME OF THE DRUG,
WHICH NAME IS PRINTED PROMINENTLY AND IN TYPE AT LEAST HALF
AS LARGE AS THAT USED FOR ANY PRINTED TRADE OR BRAND NAME OF
THE DRUG;
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