FDA Approves Merck’s ZERBAXA® (ceftolozane and tazobactam) 3g Dose for the Treatment of Adults with Hospital-Acquired and Ventilator-Associated Bacterial Pneumonia (HABP/VABP)

Dateline City:
KENILWORTH, N.J.

Approval Based on Results of Phase 3 Trial Evaluating Critically Ill Patients with Pneumonia; 100% of Patients Were on Mechanical Ventilation

KENILWORTH, N.J.–(BUSINESS WIRE)–Merck (NYSE:MRK), known as MSD outside the United States and Canada,
today announced that the U.S.

Language:
English

Contact:

Media:

Pam Eisele
(267) 305-3558

Sarra Herzog
(908) 740-1871

Investors:

Teri Loxam
(908) 740-1986

Michael DeCarbo
(908) 740-1807

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Ticker:
MRK

Exchange:
NYSE

@merck

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