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Code of Virginia

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Chapter 34.
Drug Control Act
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  • Article 1.
    General Provisions
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  • § 54.1-3400
    Citation
    § 54.1-3401
    Definitions
    § 54.1-3401.1
    Repealed
    § 54.1-3402
    Repealed
    § 54.1-3403
    Chapter not applicable to economic poisons
    § 54.1-3404
    Inventories of controlled substances required of certain persons; contents and form of record
    § 54.1-3405
    Access to and copies of records; inspections
    § 54.1-3406
    Records confidential; disclosure of information about violations of federal law
    § 54.1-3407
    Analysis of controlled substances
    § 54.1-3408
    Professional use by practitioners
    § 54.1-3408.01
    Requirements for prescriptions
    § 54.1-3408.02
    Transmission of prescriptions
    § 54.1-3408.03
    Dispensing of therapeutically equivalent drug product permitted
    § 54.1-3408.04
    Dispensing of interchangeable biosimilars permitted
    § 54.1-3408.05
    Use of FDA-approved substance upon publication of final rule
    § 54.1-3408.1
    Prescription in excess of recommended dosage in certain cases
    § 54.1-3408.2
    Failure to report administration or dispensing of or prescription for controlled substances; report required; penalty
    § 54.1-3408.3
    Certification for use of cannabis for treatment
    § 54.1-3408.4
    Expired
    § 54.1-3408.5
    Epinephrine required in certain places of public accommodation
    § 54.1-3409
    Professional use by veterinarians
    § 54.1-3410
    When pharmacist may sell and dispense drugs
    § 54.1-3410.1
    Requirements for radiopharmaceuticals
    § 54.1-3410.2
    Compounding; pharmacists' authority to compound under certain conditions; labeling and record maintenance requirements
    § 54.1-3410.3
    Accessible prescription labels
    § 54.1-3411
    When prescriptions may be refilled
    § 54.1-3411.1
    Prohibition on returns, exchanges, or re-dispensing of drugs; exceptions
    § 54.1-3411.2
    Prescription drug disposal programs
    § 54.1-3411.2:1
    Guidelines for disposal of unused drugs
    § 54.1-3412
    Date of dispensing; initials of pharmacist; automated data processing system
    § 54.1-3413
    Manufacturing and administering Schedule I drugs
    § 54.1-3414
    Official orders for Schedule II drugs
    § 54.1-3415
    Distribution of drugs in Schedules II through VI by manufacturers and wholesalers
    § 54.1-3415.1
    Delivery of medical devices on behalf of a medical equipment supplier
    § 54.1-3416
    No prescription for preparations listed pursuant to Schedule V
    § 54.1-3417
    Disposing of stocks of Schedules II through V drugs
    § 54.1-3418
    Sale of aqueous or oleaginous solutions
    § 54.1-3419
    Dispensing of insulin preparations
    § 54.1-3420
    Distribution of certain drugs; written request or confirmation of receipt
    § 54.1-3420.1
    Identification required for filling prescriptions
    § 54.1-3420.2
    Delivery of prescription drug order
    § 54.1-3420.3
    Prohibition on refusing to fill prescription from telemedicine provider
    § 54.1-3421
    New drugs
    § 54.1-3422
    Controlled substances registration certificate required in addition to other requirements; exemptions
    § 54.1-3423
    Board to issue registration unless inconsistent with public interest; authorization to conduct research; application and fees
    § 54.1-3424
    Suspension or revocation of registration, license or permit; limitation to particular controlled substance; controlled substances placed under seal; sale of perishables and forfeiture; notification to DEA
    § 54.1-3425
    Repealed
    § 54.1-3426
    Regulations for special packaging
    § 54.1-3427
    Dispensing drugs without safety closure container
    § 54.1-3428
    Dissemination of information
    § 54.1-3429
    Revocation of permit issued to manufacturer, wholesaler or distributor
    § 54.1-3430
    Display of permit; permits nontransferable; renewal
    § 54.1-3431
    Admission into evidence of certain certificates of analysis
  • Article 4.
    Permitting of Manufacturers
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  • § 54.1-3437
    Permit to manufacture drugs
    § 54.1-3437.1
    Limited permit for repackaging drugs
    § 54.1-3438
    Manufacturing, etc., of drugs or proprietary medicines, to be supervised by pharmacist
    § 54.1-3439
    Application for nonrestricted manufacturing permit; fee
    § 54.1-3440
    Persons to whom nonrestricted permit is granted
    § 54.1-3441
    Restricted manufacturing permit; application; fee; separate application and permit for each place of manufacturing
    § 54.1-3442
    When permit not to be granted; regulations
    § 54.1-3442.01
    Registration of nonresident manufacturer; renewal
    § 54.1-3442.02
    Prescription drug price transparency
  • Article 4.1.
    Expanded Access to Investigational Drugs, Biological Products, and Devices
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  • § 54.1-3442.1
    Definitions
    § 54.1-3442.2
    Eligibility for expanded access to investigational drugs, biological products, and devices; written, informed consent to treatment
    § 54.1-3442.3
    Expanded access to investigational drugs, biological products, or devices; cost; insurance coverage
    § 54.1-3442.4
    Limitation of liability
  • Article 7.
    Controlled Paraphernalia
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  • § 54.1-3466
    Possession or distribution of controlled paraphernalia; definition of controlled paraphernalia; evidence; exceptions
    § 54.1-3467
    Distribution of hypodermic needles or syringes, gelatin capsules, quinine or any of its salts
    § 54.1-3468
    Conditions to dispensing device, item, or substance; records
    § 54.1-3469
    Storage, usage, and disposition of controlled paraphernalia
    § 54.1-3470
    Obtaining controlled paraphernalia by fraud, etc.
    § 54.1-3471
    Issuance of permits to certain persons other than registered pharmacists
    § 54.1-3472
    Article inapplicable to certain persons