United States · FDA National Drug Code directory

VASOPRESSIN

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
51662-1623_39ae8951-80f9-e2c7-e063-6294a90a4f43
Product NDC
51662-1623
Form
INJECTION
Composition / generic term
VASOPRESSIN
Labeler
HF Acquisition Co LLC, DBA HealthFirst
Marketing category
ANDA
Marketing start / end (source format)
20230302
Source listing expiry
20261231

Source-listed ingredients

  • VASOPRESSIN, UNSPECIFIED — 20 [USP'U]/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 mL in 1 VIAL, MULTI-DOSE (51662-1623-1) · 51662-1623-1
  • 1 VIAL, MULTI-DOSE in 1 POUCH (51662-1623-2) / 1 mL in 1 VIAL, MULTI-DOSE · 51662-1623-2

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.

Browse United States records →