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Prescription medicine

Ceftazidime, avibactam

Official FDA data, not advice

Everything here comes from the U.S. Food and Drug Administration (FDA): the drug label, the NDC Directory, Drugs@FDA, recall reports and the drug shortage list. Each fact shows its source and date.

This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.

In an emergency, call 911. If someone may have taken too much of a medicine, call Poison Help: 1‑800‑222‑1222.

Quick answers

What is Ceftazidime, avibactam used for?
The FDA-approved label (Avycaz, Allergan, Inc., April 30, 2025) says: “AVYCAZ is a combination of ceftazidime, a cephalosporin, and avibactam, a beta-lactamase inhibitor, indicated for the treatment of the following infections caused by designated susceptible Gram-negative microorganisms in adult and pediatric patients (at least 31 weeks gestational age) …” This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.
Does Ceftazidime, avibactam have a boxed warning?
No. None of the 1 FDA labels we found for this medicine has a boxed warning.
Is there a shortage of Ceftazidime, avibactam?
No current shortage is listed by the FDA for the products of this medicine (FDA data from October 30, 2026).
Has Ceftazidime, avibactam been recalled?
No recall linked to the products of this medicine appears in the FDA enforcement reports we use.
Who makes Ceftazidime, avibactam?
1 company lists prescription products of Ceftazidime, avibactam in the FDA NDC Directory, including Allergan, Inc..

What Ceftazidime, avibactam is used for

Quoted from the “Indications and Usage” section of the FDA-approved label.

AVYCAZ is a combination of ceftazidime, a cephalosporin, and avibactam, a beta-lactamase inhibitor, indicated for the treatment of the following infections caused by designated susceptible Gram-negative microorganisms in adult and pediatric patients (at least 31 weeks gestational age) …

— FDA label: Avycaz, Allergan, Inc., effective April 30, 2025. Read the full label on DailyMed →

This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.

Conditions named on the label

These condition names appear word for word in the label’s “Indications and Usage” text (matched with a reviewed table). Each page lists hospitals whose own websites name the condition.

Related medical specialties

Boxed warning

A boxed warning (“black box”) is the FDA’s strongest warning on a drug label, for serious or life-threatening risks.

The label quoted above has no boxed warning.

Forms and how it is given

Dosage formsPowder, for solution
RouteIntravenous
Prescription products1 in the FDA NDC Directory
Brand namesAvycaz

Companies that list this medicine

Labelers in the FDA NDC Directory: the company named on the package (maker or distributor), with the number of prescription products.

FDA approval history

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
Brand and biologic applications
ApplicationSponsorApprovedLater changes approved
NDA206494
AVYCAZ
AbbvieFebruary 25, 2015 11, latest April 25, 2025
2025: Labeling · 2025: Labeling · 2024: Efficacy

Shortage status

The FDA drug shortage list does not show these products.

FDA Drug Shortages database →

Recalls

No recall linked to these products (by their NDC code) appears in the FDA enforcement reports.

Official identifiers

RxCUI (RxNorm)1603840, 1603845
SPL set ID of the quoted labeld9c2803f-dc9c-4b19-b4a3-8303bc8c15fd
FDA labels (SPL)1
FDA applicationsNDA206494
Active ingredients (FDA)AVIBACTAM / CEFTAZIDIME

Sources

  1. FDA-approved label on DailyMed (National Library of Medicine) — Avycaz, Allergan, Inc., effective April 30, 2025; via openFDA, FDA data exported October 30, 2026, retrieved October 31, 2026
  2. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  4. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
  5. Drug shortages (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026

openFDA data is provided by the FDA as is; it may be incomplete. Always rely on the label that comes with your medicine. FDA Enforcement Report search →

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