United States · FDA National Drug Code directory

Desmopressin Acetate

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
39822-6250_0ec4ffe1-0ee2-fc69-e063-6394a90ab7fb
Product NDC
39822-6250
Form
INJECTION, SOLUTION
Composition / generic term
desmopressin acetate
Labeler
XGen Pharmaceuticals DJB, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20240322
Source listing expiry
20261231

Source-listed ingredients

  • DESMOPRESSIN ACETATE — 4 ug/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 VIAL in 1 CARTON (39822-6250-1) / 10 mL in 1 VIAL · 39822-6250-1

Source and coverage

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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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