United States · FDA National Drug Code directory

ZINPLAVA

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
0006-3025_12338d29-efb0-4943-b5f5-826350e9ec46
Product NDC
0006-3025
Form
INJECTION, SOLUTION
Composition / generic term
bezlotoxumab
Labeler
Merck Sharp & Dohme LLC
Marketing category
BLA
Marketing start / end (source format)
20161021
Source listing expiry
20261231

Source-listed ingredients

  • BEZLOTOXUMAB — 25 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 VIAL, SINGLE-DOSE in 1 CARTON (0006-3025-00) / 40 mL in 1 VIAL, SINGLE-DOSE (0006-3025-01) · 0006-3025-00

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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