New York Laws
Article 137 - Pharmacy
6801 - Definition of Practice of Pharmacy.

(a) report such administration by electronic transmission or facsimile
to the patient's attending primary health care practitioner or
practitioners, if any, and, to the extent practicable, make himself or
herself available to discuss the outcome of such immunization, including
any adverse reactions, with the attending primary health care
practitioner, and to the statewide immunization registry or the citywide
immunization registry, as established pursuant to and to the extent
permitted by section twenty-one hundred sixty-eight of the public health
law; and
(b) provide information to the patient or, where applicable, the
person legally responsible for the patient, on the importance of having
a primary health care practitioner, developed by the commissioner of
health; and
(c) report such administration, absent of any individually
identifiable health information, to the department of health in a manner
required by the commissioner of health; and
(d) prior to administering the immunization, inform the patient or,
where applicable, the person legally responsible for the patient, of the
total cost of the immunization or immunizations, subtracting any health
insurance subsidization, if applicable. In the case the immunization is
not covered, the pharmacist must inform the patient or, where
applicable, the person legally responsible for the patient, of the
possibility that the immunization may be covered when administered by a
primary care physician or practitioner; and
(e) administer the immunization or immunizations according to the most
current recommendations by the advisory committee for immunization
practices (ACIP), provided however, that a pharmacist may administer any
immunization authorized under this section when specified by a patient
specific order.
3. No pharmacist shall administer immunizing agents without receiving
training satisfactory to the commissioner and the commissioner of health
which shall include, but not be limited to, techniques for screening
individuals and obtaining informed consent; techniques of
administration; indications, precautions and contraindications in the
use of agent or agents; record keeping of immunization and information;
and handling emergencies, including anaphylaxis and needlesticks.
4. When administering an immunization in a pharmacy, the licensed
pharmacist shall provide an area for the immunization that provides for
a patient's privacy. The privacy area should include:
a. a clearly visible posting of the most current "Recommended Adult
Immunization Schedule" published by the advisory committee for
immunization practices (ACIP); and
(b) education materials on influenza vaccinations for children as
determined by the commissioner and the commissioner of health.
5. A licensed pharmacist may execute a non-patient specific order, for
dispensing up to a seven day starter pack of HIV post-exposure
prophylaxis medications for the purpose of preventing human

immunodeficiency virus infection, by a physician licensed in this state
or nurse practitioner certified in this state, pursuant to rules and
regulations promulgated by the commissioner in consultation with the
commissioner of health following a potential human immunodeficiency
virus exposure.
6. A licensed pharmacist may execute a non-patient-specific regimen of
insulin and related supplies to an individual who has a valid
prescription for insulin and related supplies which has since expired
within the last twelve months. The valid prescription must have been
prescribed or ordered by a physician licensed in this state or nurse
practitioner certified in this state. Execution of a
non-patient-specific regimen shall be on an emergency basis provided the
pharmacist:
(a) first attempts to obtain an authorization from the prescriber of
the patient-specific prescription and cannot obtain the authorization,
and the prescriber does not object to dispensing to the patient under
the non-patient-specific regimen;
(b) provides a refill of the patient-specific prescription and the
quantity of that refill is in conformity with the directions for use
under the patient-specific prescription, but limited to an amount not to
exceed a thirty-day emergency supply; and
(c) notifies, within seventy-two hours of dispensing the refill or
refills, the prescriber of the patient-specific prescription whose
authorization could not be obtained, that an emergency prescription of
insulin has been dispensed.
* 7. A licensed pharmacist is a qualified health care professional
under section five hundred seventy-one of the public health law for the
purposes of directing a limited service laboratory and ordering and
administering COVID-19 and influenza tests authorized by the Food and
Drug Administration (FDA), subject to certificate of waiver requirements
established pursuant to the federal clinical laboratory improvement act
of nineteen hundred eighty-eight.
* NB Repealed April 9, 2024
* 8. A licensed pharmacist within their lawful scope of practice may
administer injectable medications into the deltoid muscle, pursuant to
section six thousand eight hundred two of this article, for the
treatment of mental health and substance use disorder, as prescribed or
ordered by a licensed prescriber, acting within their scope of practice
in this state and in accordance with regulations, including but not
limited to regulations promulgated by the commissioner in consultation
with any other state agencies, as necessary.
* NB Effective December 28, 2023
* 9. a. A licensed pharmacist may execute a non-patient specific order
for the dispensing of self-administered hormonal contraceptives
prescribed or ordered by the commissioner of health, a physician
licensed in this state or a nurse practitioner certified in this state
pursuant to rules and regulations promulgated by the commissioner.
b. Prior to dispensing self-administered hormonal contraceptives to a
patient, and at a minimum of every twelve months for each returning
patient, the pharmacist shall:
(i) provide the patient with a self-screening risk assessment
questionnaire, developed by the commissioner of health in consultation
with the commissioner, to be reviewed by the pharmacist to identify any
known risk factors and assist the patient's selection of an appropriate
self-administered hormonal contraceptive; and
(ii) provide the patient with a fact sheet, developed by the
commissioner of health, that includes but is not limited to, the
clinical considerations and recommendations for use of the

self-administered hormonal contraceptive, the appropriate method for
using such hormonal contraceptive, information on the importance of
follow-up health care, health care referral information, and the ability
of the patient to opt out of practitioner reporting requirements.
c. No pharmacist shall dispense self-administered hormonal
contraceptives under this subdivision without receiving training
satisfactory to the commissioner.
d. A pharmacist shall notify the patient's primary health care
practitioner, unless the patient opts out of such notification, within
seventy-two hours of dispensing a self-administered hormonal
contraceptive, that such self-administered hormonal contraceptive has
been dispensed. If the patient does not have a primary health care
practitioner, or is unable to provide contact information for their
primary health care practitioner, the pharmacist shall provide the
patient with a written record of the contraceptives dispensed, and
advise the patient to consult an appropriate health care practitioner.
e. Nothing in this subdivision shall prevent a pharmacist from
refusing to dispense a non-patient specific order of self-administered
hormonal contraceptive pursuant to this subdivision if, in their
professional judgment, potential adverse effects, interactions or other
therapeutic complications could endanger the health of the patient.
* NB Effective November 2, 2024

Structure New York Laws

New York Laws

EDN - Education

Title 8 - The Professions

Article 137 - Pharmacy

6800 - Introduction.

6801 - Definition of Practice of Pharmacy.

6801-A - Collaborative Drug Therapy Management Demonstration Program.

6802 - Definitions.

6803 - Practice of Pharmacy and Use of Title "Pharmacist".

6804 - State Board of Pharmacy.

6805 - Requirements for a Professional License.

6806 - Limited Permits.

6807 - Exempt Persons; Special Provisions.

6808 - Registering and Operating Establishments.

6808-A - Identification of Pharmacists.

6808-B - Registration of Nonresident Establishments.

6810 - Prescriptions.

6811 - Misdemeanors.

6811-A - Certain Drugs to Be Clearly Marked or Labeled.

6811-B - Door-to-Door Distribution of Drugs Prohibited.

6811-C - Patient Notification of Recalled Drugs.

6812 - Special Provisions.

6813 - Seizure:

6814 - Records of Shipment.

6815 - Adulterating, Misbranding and Substituting.

6816 - Omitting to Label Drugs, or Labeling Them Wrongly.

6816-A - When Substitution Is Required.

6817 - New Drugs.

6818 - Adulterated and Misbranded Cosmetics.

6818-A - Cosmetic Samples.

6819 - Regulations Making Exceptions.

6820 - Certification of Coal-Tar Colors for Drugs and Cosmetics.

6821 - Poison Schedules; Register.

6822 - Examinations and Investigations.

6823 - Factory Inspection.

6824 - Injunction Proceedings.

6825 - Proof Required in Prosecution for Certain Violations.

6826 - Drug Retail Price Lists.

6826-A - Reducing Certain Copayments.

6827 - Mandatory Continuing Education.

6828 - Certificates of Administration.

6829 - Interpretation and Translation Requirements for Prescription Drugs and Standardized Medication Labeling.

6830 - Standardized Patient-Centered Data Elements.

6831 - Special Provisions Relating to Outsourcing Facilities.

6832 - Limitations on Assistance of an Unlicensed Person.