NDC 0338-9640 – Vasopressin in 0.9% Sodium Chloride

Vasopressin 20 [USP'U]/100mL · Injection · Intravenous

Human Prescription Drug 2 recalls

Product NDC0338-9640

Product details

Brand name
Vasopressin in 0.9% Sodium Chloride
Generic name
Vasopressin in 0.9% Sodium Chloride
Labeler
Baxter Healthcare Corporation
Dosage form
Injection
Route
Intravenous
Marketing category
NDA · NDA217569
Marketed since
September 29, 2023
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Vasopressin in 0.9% Sodium Chloride →

Package NDC codes (1)

Package NDCDescriptionSince
0338-9640-1212 BAG in 1 CARTON (0338-9640-12) / 100 mL in 1 BAGSep 29, 2023

Recalls mentioning this NDC

Other Vasopressin in 0.9% Sodium Chloride products