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71 chapters · 1,802 sections in this title.
SDCL § 36-11-46.4 Standards for selecting prescription drug
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A pharmacist may not select a product unless it has been manufactured, labeled, or distributed by a manufacturer, labeler, or distributor who: (1) Marks capsules and tablets with an identification code or monogram; (2) Labels products with their expiration date; (3) Provides reas…
SDCL § 36-11-46.5 Liability for dispensing equivalent drug product or interchangeable biological product
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A pharmacist who selects an equivalent drug product or interchangeable biological product pursuant to this chapter assumes no greater liability for selecting the dispensed drug or biological product than would be incurred in filling a prescription for a drug or biological product…
SDCL § 36-11-46.6 Label to contain drug name--Form when generic equivalent selected--Contents of prescription files--Label information
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The pharmacist shall, unless otherwise instructed by the prescriber, label the prescription container with the name of the dispensed drug. If the dispensed drug does not have a brand name, the prescription label shall indicate the generic name or the United States Pharmacopoeia p…
SDCL § 36-11-46.7 Equivalent drug and biological product requirements not applicable to hospital patients
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The requirements of §§ 36-11-46.1 to 36-11-46.3 , inclusive, 36-11-46.6 , and 36-11-46.9 to 36-11-46.11 , inclusive, do not apply to an order to dispense a drug or biological product to a hospital patient. Source: SL 1990, ch 306 , § 6; SL 1993, ch 277 , § 6; SL 2018, ch 231 , § …
