ASTRAZENECA COVID-19 VACCINE

Manufacturer
AstraZeneca Pharmaceuticals LP | AstraZeneca PLC
Effective date
2020-12-22
Label type
VACCINE LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:00:04

Label at a glance#

ProductASTRAZENECA COVID-19 VACCINE
Active ingredientAZD-1222
Label structure2 sections

Label contents#

Full prescribing information#

Package/Label Display Panel – Vial Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

AstraZeneca COVID-19 Vaccine                         NDC 0310-1222-10

For use under Emergency Use Authorization

Suspension for Intramuscular Injection

After first use, discard after:

6 hours at 20°-25°C (68°-77°F), or

48 hours at 2°-8°C (36°-46°F)

For Exp Date: see

www.azcovid-19.com

Multi-dose vial (10 doses of 0.5 mL)

vial_label_5ml
vial_label_5ml

Package/Label Display Panel – Vial Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 0310-1222-15

AstraZeneca COVID-19 Vaccine

For use under Emergency Use Authorization

Suspension for Intramuscular Injection

Store at 2°-8°C (36°-46°F) in original carton to protect from light.

Do not freeze or shake. No preservative.

Discard 6 hours after first use when held at 20°-25°C (68°-77°F).

Discard 48 hours after first use when held at 2°-8°C (36°-46°F).

10 Multi-dose vials

(each vial contains 10 doses of 0.5 mL)

AstraZeneca

carton_label
carton_label

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0310-1222-10ML - Milliliter0310-1222e62cfbd2-1a13-4a1f-a2e3-498d5512701c12021-01-08
0310-1222-15ML - Milliliter0310-1222f32e6be6-58dc-4227-88de-911945590d6812021-01-08

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0310-12220310-1222-10, 0310-1222-15

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.