Summary & Overview
CPT 91322: SARS–CoV–2 Vaccine, 50 mcg/0.5 mL Intramuscular
CPT code 91322 identifies a SARS–CoV–2 vaccine product administered intramuscularly at a dosage of 50 mcg/0.5 mL to reduce risk of COVID–19. This vaccine code matters nationally as COVID–19 vaccination remains a central public health activity with broad payer coverage and implications for outpatient care delivery, reporting, and vaccine inventory management.
Key payers discussed include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find a concise overview of clinical context, typical sites of service, and payer scope. The publication summarizes common modifier usage patterns and highlights areas where payers have historically issued policy guidance or coverage criteria for vaccine administration services. It also outlines benchmarks and policy updates relevant to billing and reimbursement for adult and eligible population vaccination programs.
The report is intended to help billing managers, compliance officers, and clinicians understand how CPT code 91322 is used in practice, what services it represents, and where to look for payer-specific policy details. Data not available in the input for associated taxonomies, ICD-10 diagnoses, and related codes.
Billing Code Overview
CPT code 91322 represents a SARS–CoV–2 vaccine product administered by intramuscular injection to reduce the patient’s risk of contracting COVID–19. The dosage specified for this product is 50 mcg/0.5 mL.
-
Service type: Vaccine administration (intramuscular)
-
Typical site of service: Ambulatory clinics, primary care offices, mass vaccination clinics, and other outpatient settings where intramuscular vaccinations are provided.
Data not available in the input for associated taxonomies, ICD-10 diagnoses, and related codes.
Clinical & Coding Specifications
Clinical Context
A typical patient is an adult seeking COVID-19 vaccination booster dose during a routine ambulatory visit at a primary care clinic or pharmacy. The patient presents for vaccination to reduce risk of SARS–CoV–2 infection and has no acute illness contraindicating intramuscular injection. Documentation includes informed consent, vaccine manufacturer and lot number, dose 50 mcg/0.5 mL, route intramuscular (IM), administration site (e.g., left deltoid), and vaccination date and time. Pre-administration screening for allergies and recent acute illnesses is performed, and the patient is observed for the standard post-vaccination monitoring period for immediate adverse reactions. Billing uses the vaccine product code 91322 for the 50 mcg/0.5 mL SARS–CoV–2 vaccine; visit-level evaluation and management services, if provided and medically necessary, are reported separately using appropriate E/M codes with modifiers as needed.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
00 | No modifier (standard) | Used when no special circumstances apply and full payment is appropriate. |
22 |