POTASSIUM CHLORIDE- potassium chloride injection, solution, concentrate

País: Estados Unidos

Língua: inglês

Origem: NLM (National Library of Medicine)

Ingredientes ativos:

POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152)

Disponível em:

Cardinal Health

DCI (Denominação Comum Internacional):

POTASSIUM CHLORIDE

Composição:

POTASSIUM CHLORIDE 149 mg in 1 mL

Via de administração:

INTRAVENOUS

Tipo de prescrição:

PRESCRIPTION DRUG

Indicações terapêuticas:

Potassium Chloride for Injection Concentrate, USP is indicated in the treatment of potassium deficiency states when oral replacement is not feasible. Potassium Chloride for Injection Concentrate, USP is contraindicated in diseases where high potassium levels may be encountered, and in patients with hyperkalemia, renal failure and in conditions in which potassium retention is present.

Resumo do produto:

Potassium Chloride for Injection Concentrate, USP, is supplied in single-dose containers as follows: NDC Number Type Container Concentration 55154-6999-8 Overbagged with 1 vial per bag Plastic Fliptop Vials 20 mEq/10 mL 55154-2367-8 Overbagged with 1 vial per bag Plastic Fliptop Vials 40 mEq/20 mL Store at 20 to 25°C (68 to 77°F). [See USP Controlled Room Temperature.] Revised: 9/2014                                                                        EN-3583 Hospira, Inc., Lake Forest, IL 60045 USA      Repackaged By: Cardinal Health Zanesville, OH 43701 LA67240316 LA67080413

Status de autorização:

Abbreviated New Drug Application

Características técnicas

POTASSIUM CHLORIDE- POTASSIUM CHLORIDE INJECTION, SOLUTION,
CONCENTRATE
CARDINAL HEALTH
----------
POTASSIUM CHLORIDE RX ONLY
for Injection
CONCENTRATE, USP
CONCENTRATE
_MUST BE DILUTED BEFORE USE._
_FOR INTRAVENOUS INFUSION ONLY;_
_MUST BE DILUTED PRIOR TO INJECTION_.
FLIPTOP VIALS
_DESCRIPTION_
Potassium Chloride for Injection Concentrate, USP, is a sterile,
nonpyrogenic, concentrated solution of
potassium chloride, USP in water for injection administered by
intravenous infusion only after dilution
in a larger volume of fluid. They are provided in the following
variety of concentrations and sizes
comprising a choice of single-dose containers, all designed to provide
the commonly prescribed
amounts of potassium chloride for single-dose infusion after dilution
in suitable large volume
parenterals.
*
ADDITIVE SOLUTION
(CONC. & SIZE)
K
MEQ/ML
KCL
MG/ML
MOSMOL/ML
(CALC.)
10 mEq/5 mL
2
149
4
20 mEq/10 mL
2
149
4
30 mEq/15 mL
2
149
4
40 mEq/20 mL
2
149
4
The solutions contain no bacteriostat, antimicrobial agent or added
buffer (except for pH adjustment) and
each is intended only for single-dose injection (after dilution). When
smaller doses are required,
discard the unused portion. The pH is 4.6 (4.0 to 8.0).
Potassium Chloride for Injection Concentrate, USP (appropriately
diluted) is a parenteral fluid and
electrolyte replenisher.
Potassium Chloride, USP is chemically designated KCl, a white granular
powder freely soluble in
water.
The semi-rigid material used for the plastic vials is fabricated from
a specially formulated polyolefin.
It is a copolymer of ethylene and propylene. The safety of the plastic
has been confirmed by tests in
animals according to USP biological standards for plastic containers.
The container requires no vapor
barrier to maintain the proper drug concentration.
_CLINICAL PHARMACOLOGY_
Potassium is the chief cation of body cells (160 mEq/liter of
intracellular water) and is concerned with
the maintenance of body fluid composition and electrolyte balance.
Potassium participates in
carbohydrate