Comirnaty Injection, Suspension
NDC Package 0069-2609-10
Package Information
Comirnaty (covid-19 vaccine, mrna) injection is cOMIRNATY is a vaccine indicated for active immunization to prevent coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in individuals 16 years of age and older. This formulation utilizes a injection, suspension delivery system. Marketed by Pfizer Laboratories Div Pfizer Inc, this product is identified by NDC 0069-2609 and is authorized under FDA application BLA125742.
Identification & Billing
- RxCUI: 2722598 - SARS-CoV-2 (COVID-19) vaccine 2025-2026, mRNA-BNT162b2 OMICRON (LP.8.1) 0.3 ML Prefilled Syringe, 12y+
- RxCUI: 2722598 - 0.3 ML SARS-CoV-2 (COVID-19) vaccine, mRNA-BNT162b2 OMICRON (LP.8.1) 0.1 MG/ML Prefilled Syringe
- RxCUI: 2722605 - COMIRNATY 2025-2026 vaccine, 0.3 ML Prefilled Syringe, 12y+
- RxCUI: 2722605 - 0.3 ML SARS-CoV-2 (COVID-19) vaccine, mRNA-BNT162b2 OMICRON (LP.8.1) 0.1 MG/ML Prefilled Syringe [Comirnaty 2025-2026]
- RxCUI: 2722605 - 0.3 ML Comirnaty 2025-2026 0.1 MG/ML Prefilled Syringe
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 0069 - Pfizer Laboratories Div Pfizer Inc
- 0069-2609 - Comirnaty
- 0069-2609-10 - 10 VIAL, SINGLE-DOSE in 1 CARTON / .48 mL in 1 VIAL, SINGLE-DOSE (0069-2609-01)
- 0069-2609 - Comirnaty
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 0069-2609-10 identifies a specific commercial package of 10 vial, single-dose in 1 carton / .48 ml in 1 vial, single-dose (0069-2609-01) of Comirnaty, a vaccine label labeled by Pfizer Laboratories Div Pfizer Inc. This injection, suspension is formulated for intramuscular use and contains bnt-162b2 omicron (xfg) mrna as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Pfizer Laboratories Div Pfizer Inc on August 27, 2026. The current certification is valid through December 31, 2027.
How is this Pfizer Laboratories Div Pfizer Inc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 00069260910. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Labeler segment to maintain the 5-4-2 structure.