Summary & Overview
CPT 91323: mRNA COVID-19 Vaccine, 10 mcg/0.2 mL Intramuscular
CPT code 91323 designates an mRNA-based COVID-19 vaccine product supplied for intramuscular administration at a dosage of 10 micrograms per 0.2 mL. This code captures the vaccine product itself and is integral to national vaccination efforts, facilitating standardized reporting, coverage determinations, and public health tracking. Its use matters for immunization programs, payer coverage policies, and provider billing workflows across ambulatory care settings.
Key payers included in discussions of CPT code 91323 are Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find a concise national view of the code’s clinical context, common settings where the vaccine is administered, and the payer landscape relevant to coverage and claims processing. The publication provides benchmarks for utilization and reimbursement trends where available, notes on billing considerations, and summaries of recent policy updates affecting vaccine product coding and payment. Clinical context covers the mRNA platform and intramuscular route of administration, including dose specification. Data not available in the input is noted where applicable.
Billing Code Overview
CPT code 91323 represents a COVID-19 vaccine product using mRNA technology, administered intramuscularly. The listed dosage is 10 micrograms per 0.2 mL, indicating a specific vaccine formulation and measured volume for a single dose.
Service Type: Vaccination — intramuscular administration of an mRNA COVID-19 vaccine product
Typical Site of Service: Outpatient clinic, pharmacy, public health clinic, or other ambulatory vaccination settings where intramuscular immunizations are provided
Clinical & Coding Specifications
Clinical Context
A typical patient is an adult or adolescent who presents to an outpatient vaccination clinic, primary care office, occupational health clinic, pharmacy clinic, or community vaccination site for administration of a COVID-19 mRNA booster or primary series dose. The vaccine represented by 91323 is a 10 microgram (0.2 mL) intramuscular mRNA formulation given in the deltoid muscle. Workflow steps include: pre-vaccination screening for contraindications and recent COVID-19 infection, verification of immunization consent and history, documentation of vaccine lot number and expiration, preparation of the 0.2 mL dose per manufacturer instructions, administration via intramuscular injection, monitoring the patient for immediate adverse reactions for at least 15 minutes (longer if history of anaphylaxis), post-vaccination counseling including expected local and systemic reactions, and entry of the immunization into the patient’s electronic medical record and any required immunization registry. Typical sites of service are outpatient clinics, pharmacies, community vaccination sites, and primary care or pediatric offices. Common patient scenarios include routine booster dose administration, completion of a primary series for eligible patients, and administration in medically high-risk individuals per current public health guidance.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
00 | No modifier | Use when no special modifier applies to the vaccine administration claim |