NDC Code(s) : 55154-7325-0
Packager : Cardinal Health

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Potassium ChloridePotassium Chloride POWDER, FOR SOLUTION
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:55154-7325(NDC:76439-343)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
POTASSIUM CHLORIDE(UNII: 660YQ98I10)
(POTASSIUM CATION - UNII:295O53K152) 		POTASSIUM CHLORIDE1.5 g in 1.74 g
Inactive Ingredients
Ingredient Name Strength
FD&C YELLOW NO. 6(UNII: H77VEI93A8)
MALIC ACID(UNII: 817L1N4CKP)
NEOTAME(UNII: VJ597D52EX)
SILICON DIOXIDE(UNII: ETJ7Z6XBU4)
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:55154-7325-010 in 1 BAG
11.74 g in 1 POUCH Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
Unapproved drug other 10/09/2013

PRINCIPAL DISPLAY PANEL

Potassium Chloride Powder

20 mEq

Potassium Chloride for Oral Solution, USP

10 Packets

bag label