Potassium Chloride (Page 2 of 2)

SAMPLE PACKAGE LABEL

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POTASSIUM CHLORIDE potassium chloride injection, solution, concentrate
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:52584-965(NDC:63323-965)
Route of Administration INTRAVENOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
POTASSIUM CHLORIDE (Potassium Cation) Potassium Cation 2 meq in 1 mL
Inactive Ingredients
Ingredient Name Strength
POTASSIUM HYDROXIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:52584-965-05 1 VIAL, SINGLE-DOSE in 1 BAG contains a VIAL, SINGLE-DOSE
1 5 mL in 1 VIAL, SINGLE-DOSE This package is contained within the BAG (52584-965-05)
2 NDC:52584-965-10 1 VIAL, SINGLE-DOSE in 1 BAG contains a VIAL, SINGLE-DOSE
2 10 mL in 1 VIAL, SINGLE-DOSE This package is contained within the BAG (52584-965-10)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA088901 08/01/2010
Labeler — General Injectables & Vaccines, Inc (108250663)

Revised: 11/2021 General Injectables & Vaccines, Inc

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