VASOPRESSIN

NDC 51662-1682 · HF Acquisition Co LLC, DBA HealthFirst

Generic nameVASOPRESSIN

Dosage formINJECTION, SOLUTION

RouteINTRAVENOUS

Active ingredient(s)VASOPRESSIN

Strength20 [USP'U]/mL

Pharmacologic classDecreased Diuresis [PE], Vasoconstriction [PE], Vasopressins [CS]

Marketing categoryNDA

Packages

51662-1682-2 — 1 VIAL in 1 POUCH (51662-1682-2) / 10 mL in 1 VIAL (51662-1682-1)

FDA lists these products with the same active ingredient.

0338-9640 — Vasopressin in 0.9% Sodium Chloride, 0338-9647 — Vasopressin in 0.9% Sodium Chloride, 0517-1020 — Vasopressin, 0517-1030 — Vasopressin, 0548-9701 — Vasopressin, 25021-474 — Vasopressin, 51662-1688 — VASOPRESSIN, 55150-370 — VASOPRESSIN, 63323-930 — VASOPRESSIN, 65219-039 — VASOPRESSIN, 68083-520 — Vasopressin, 68083-663 — Vasopressin, 70121-1642 — vasopressin, 71872-7306 — VASOPRESSIN, 72572-860 — Vasopressin, 81298-8552 — Vasopressin, 81298-8554 — Vasopressin, 84549-370 — VASOPRESSIN

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.