United States · FDA National Drug Code directory

Barhemsys

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
71390-125_65f9d1f3-9e6a-48bd-8ae3-fee41402cd36
Product NDC
71390-125
Form
INJECTION, SOLUTION
Composition / generic term
Amisulpride
Labeler
Acacia Pharma Ltd
Marketing category
NDA
Marketing start / end (source format)
20200227 / 20301130

Source-listed ingredients

  • AMISULPRIDE — 2.5 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 10 CARTON in 1 PACKAGE (71390-125-20) / 1 VIAL, SINGLE-DOSE in 1 CARTON (71390-125-21) / 2 mL in 1 VIAL, SINGLE-DOSE · 71390-125-20
  • 10 CARTON in 1 PACKAGE (71390-125-50) / 1 VIAL, SINGLE-DOSE in 1 CARTON (71390-125-51) / 4 mL in 1 VIAL, SINGLE-DOSE · 71390-125-50

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 →