21 CFR 1306.05 - Manner of issuance of prescriptions.
(a) All prescriptions for controlled substances shall be dated as of, and signed on, the day when issued and shall bear the full name and address of the patient, the drug name, strength, dosage form, quantity prescribed, directions for use, and the name, address and registration number of the practitioner.
(b) A prescription for a Schedule III, IV, or V narcotic drug approved by FDA specifically for “detoxification treatment” or “maintenance treatment” must include the identification number issued by the Administrator under § 1301.28(d) of this chapter or a written notice stating that the practitioner is acting under the good faith exception of § 1301.28(e) of this chapter.
(c) Where a prescription is for gamma-hydroxybutyric acid, the practitioner shall note on the face of the prescription the medical need of the patient for the prescription.
(d) A practitioner may sign a paper prescription in the same manner as he would sign a check or legal document (e.g., J.H. Smith or John H. Smith). Where an oral order is not permitted, paper prescriptions shall be written with ink or indelible pencil, typewriter, or printed on a computer printer and shall be manually signed by the practitioner. A computer-generated prescription that is printed out or faxed by the practitioner must be manually signed.
(f) A prescription may be prepared by the secretary or agent for the signature of a practitioner, but the prescribing practitioner is responsible in case the prescription does not conform in all essential respects to the law and regulations. A corresponding liability rests upon the pharmacist, including a pharmacist employed by a central fill pharmacy, who fills a prescription not prepared in the form prescribed by DEA regulations.
(g) An individual practitioner exempted from registration under § 1301.22(c) of this chapter shall include on all prescriptions issued by him the registration number of the hospital or other institution and the special internal code number assigned to him by the hospital or other institution as provided in § 1301.22(c) of this chapter, in lieu of the registration number of the practitioner required by this section. Each paper prescription shall have the name of the practitioner stamped, typed, or handprinted on it, as well as the signature of the practitioner.
(h) An official exempted from registration under § 1301.23(a) of this chapter must include on all prescriptions issued by him his branch of service or agency (e.g., “U.S. Army” or “Public Health Service”) and his service identification number, in lieu of the registration number of the practitioner required by this section. The service identification number for a Public Health Service employee is his Social Security identification number. Each paper prescription shall have the name of the officer stamped, typed, or handprinted on it, as well as the signature of the officer.
- 21 CFR 1306.25 — Transfer Between Pharmacies of Prescription Information for Schedules III, IV, and v Controlled Substances for Refill Purposes.
- 21 CFR 1311.300 — Application Provider Requirements - Third-Party Audits or Certifications.
- 21 CFR 1311.120 — Electronic Prescription Application Requirements.
- 21 CFR 1306.15 — Provision of Prescription Information Between Retail Pharmacies and Central Fill Pharmacies for Prescriptions of Schedule II Controlled Substances.
- 21 CFR 1311.205 — Pharmacy Application Requirements.
- 21 CFR 1311.140 — Requirements for Signing a Controlled Substance Prescription.
- 21 CFR 1311.102 — Practitioner Responsibilities.
- 21 CFR 1306.08 — Electronic Prescriptions.
- 21 CFR 1306.27 — Provision of Prescription Information Between Retail Pharmacies and Central Fill Pharmacies for Initial and Refill Prescriptions of Schedule III, IV, or v Controlled Substances.
- 21 CFR 1306.11 — Requirement of Prescription.
- 21 CFR 1311.200 — Pharmacy Responsibilities.