This text of Iowa § 124.552 (Information reporting) is published on Counsel Stack Legal Research, covering Iowa primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.
1.Unless otherwise prohibited by federal or state law, each licensed pharmacy that
dispenses controlled substances identified pursuant to section 124.554, subsection 1,
paragraph “g”, to patients in the state, each licensed pharmacy located in the state that
dispenses such controlled substances identified pursuant to section 124.554, subsection 1,
paragraph “g”, to patients inside or outside the state, unless specifically excepted in this
section or by rule, and each prescribing practitioner furnishing, dispensing, or supplying
controlled substances to the prescribing practitioner’s patient, shall submit the following
prescription information to the program:
a.Pharmacy identification.
b.Patient identification.
c.Prescribing practitioner identification.
d.The date the prescription was
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1. Unless otherwise prohibited by federal or state law, each licensed pharmacy that
dispenses controlled substances identified pursuant to section 124.554, subsection 1,
paragraph “g”, to patients in the state, each licensed pharmacy located in the state that
dispenses such controlled substances identified pursuant to section 124.554, subsection 1,
paragraph “g”, to patients inside or outside the state, unless specifically excepted in this
section or by rule, and each prescribing practitioner furnishing, dispensing, or supplying
controlled substances to the prescribing practitioner’s patient, shall submit the following
prescription information to the program:
a. Pharmacy identification.
b. Patient identification.
c. Prescribing practitioner identification.
d. The date the prescription was issued by the prescribing practitioner.
e. The date the prescription was dispensed.
f. An indication of whether the prescription dispensed is new or a refill.
g. Identification of the drug dispensed.
h. Quantity of the drug dispensed.
i. The number of days’ supply of the drug dispensed.
j. Serial or prescription number assigned by the pharmacy.
k. Type of payment for the prescription.
l. Other information identified by the board by rule.
2. Information shall be submitted electronically in a secure format specified by the board
unless the board has granted a waiver and approved an alternate secure format.
3. Information shall be timely transmitted within one business day of the dispensing of
the controlled substance, unless the board grants an extension. The board may grant an
extension if either of the following occurs:
a. The pharmacy or prescribing practitioner suffers a mechanical or electronic failure, or
cannot meet the deadline established by the board for other reasons beyond the pharmacy’s
or practitioner’s control.
b. The board is unable to receive electronic submissions.
4. This section shall not apply to dispensing by a licensed pharmacy for the purposes of
inpatient hospice care or long-term residential facility patient care.