VASOPRESSIN (Page 3 of 3)

PRINCIPAL DISPLAY PANEL — NDC: 42367-570-22 — Vial Label

vial label
(click image for full-size original)

VASOPRESSIN
vasopressin injection
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:42367-570
Route of Administration PARENTERAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
VASOPRESSIN (VASOPRESSIN) VASOPRESSIN 20 U in 1 mL
Inactive Ingredients
Ingredient Name Strength
CHLOROBUTANOL HEMIHYDRATE
WATER
ACETIC ACID
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:42367-570-87 25 VIAL, MULTI-DOSE in 1 CARTON contains a VIAL, MULTI-DOSE (42367-570-22)
1 NDC:42367-570-22 1 mL in 1 VIAL, MULTI-DOSE This package is contained within the CARTON (42367-570-87)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA211538 01/10/2022 06/30/2024
Labeler — Eagle Pharmaceuticals, Inc. (849818161)
Establishment
Name Address ID/FEI Operations
Curia New Mexico, LLC 078268825 MANUFACTURE (42367-570), ANALYSIS (42367-570)

Revised: 03/2023 Eagle Pharmaceuticals, Inc.

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