Potassium Chloride in Dextrose and Sodium Chloride (Page 4 of 4)

PRINCIPAL DISPLAY PANEL — 1000 mL Bag Label — IM-0090

10 mEq POTASSIUM

1000 mL

NDC 0409-7993-09

10 mEq

POTASSIUM
CHLORIDE

in 5% Dextrose and
0.45% Sodium Chloride
Injection, USP

EACH 100 mL CONTAINS POTASSIUM
CHLORIDE 74.5 mg; SODIUM CHLORIDE 450 mg;
DEXTROSE, HYDROUS 5 g IN WATER FOR
INJECTION. MAY CONTAIN HCl FOR pH
ADJUSTMENT.

ELECTROLYTES PER 1000 mL (NOT INCLUDING
IONS FOR pH ADJUSTMENT): POTASSIUM
10 mEq; SODIUM 77 mEq; CHLORIDE 87 mEq.

426 mOsmol/LITER (CALC.)
pH 4.2 (3.5 to 6.5)

ADDITIVES MAY BE INCOMPATIBLE.
CONSULT WITH PHARMACIST, IF AVAILABLE.
WHEN INTRODUCING ADDITIVES,
USE ASEPTIC TECHNIQUE, MIX THOROUGHLY
AND DO NOT STORE.

SINGLE-DOSE CONTAINER. FOR I.V. USE.
USUAL DOSAGE: SEE INSERT. STERILE,
NONPYROGENIC. USE ONLY IF SOLUTION IS
CLEAR AND CONTAINER IS UNDAMAGED.
MUST NOT BE USED IN SERIES CONNECTIONS.

Rx ONLY

3
v
CONTAINS
DEHP

PRINTED IN USA

©HOSPIRA 2004IM-0090 (4/04)

HOSPIRA, INC., LAKE FOREST, IL 60045 USA

Hospira

PRINCIPAL DISPLAY PANEL -- 1000 mL Bag Label -- IM-0090
(click image for full-size original)

PRINCIPAL DISPLAY PANEL — 500 mL Bag Label — IM-0057

10 mEq POTASSIUM

500 mL

NDC 0409-7901-03

10 mEq

POTASSIUM
CHLORIDE
in 5% Dextrose and
0.225% Sodium Chloride Inj., USP

EACH 100 mL CONTAINS POTASSIUM CHLORIDE 149 mg; SODIUM
CHLORIDE 225 mg; DEXTROSE, HYDROUS 5 g IN WATER FOR INJECTION.
MAY CONTAIN HCl FOR pH ADJUSTMENT. ELECTROLYTES PER 1000 mL
(NOT INCLUDING IONS FOR pH ADJUSTMENT): POTASSIUM 20 mEq;
SODIUM 38.5 mEq; CHLORIDE 58.5 mEq. 370 mOsmol/LITER (CALC.)
pH 4.2 (3.5 to 6.5)

ADDITIVES MAY BE INCOMPATIBLE. CONSULT WITH
PHARMACIST, IF AVAILABLE. WHEN INTRODUCING
ADDITIVES, USE ASEPTIC TECHNIQUE, MIX
THOROUGHLY AND DO NOT STORE.

SINGLE-DOSE CONTAINER. FOR I.V. USE. USUAL DOSAGE: SEE INSERT.
STERILE, NONPYROGENIC. USE ONLY IF SOLUTION IS CLEAR AND
CONTAINER IS UNDAMAGED. MUST NOT BE USED IN SERIES
CONNECTIONS.

©HOSPIRA 2004
IM-0057 (4/04)
PRINTED IN USA
HOSPIRA, INC., LAKE FOREST, IL 60045 USA

3
vCONTAINS DEHP

Rx ONLY

Hospira

PRINCIPAL DISPLAY PANEL -- 500 mL Bag Label -- IM-0057
(click image for full-size original)

PRINCIPAL DISPLAY PANEL — 500 mL Bag Label — IM-0096

10 mEq POTASSIUM

500 mL

NDC 0409-7998-03

10 mEq

POTASSIUM
CHLORIDE
in 5% Dextrose and
0.3% Sodium Chloride Inj., USP

EACH 100 mL CONTAINS POTASSIUM CHLORIDE 149 mg; SODIUM
CHLORIDE 300 mg; DEXTROSE, HYDROUS 5 g IN WATER FOR
INJECTION. MAY CONTAIN HCl FOR pH ADJUSTMENT.
ELECTROLYTES PER 1000 mL (NOT INCLUDING IONS FOR pH
ADJUSTMENT): POTASSIUM 20 mEq; SODIUM 51 mEq; CHLORIDE 71
mEq. 395 mOsmol/LITER (CALC.)
pH 4.2 (3.5 to 6.5)

ADDITIVES MAY BE INCOMPATIBLE.
CONSULT WITH PHARMACIST, IF AVAILABLE.
WHEN INTRODUCING ADDITIVES, USE ASEPTIC TECHNIQUE, MIX
THOROUGHLY AND DO NOT STORE.

SINGLE-DOSE CONTAINER. FOR I.V. USE. USUAL DOSAGE: SEE
INSERT. STERILE, NONPYROGENIC. USE
ONLY IF SOLUTION IS CLEAR AND
CONTAINER IS UNDAMAGED. MUST NOT
BE USED IN SERIES CONNECTIONS.

3
v
CONTAINS DEHP

PRINTED IN USA
Rx ONLY

©HOSPIRA 2004IM-0096 (4/04)

HOSPIRA, INC., LAKE FOREST, IL 60045 USA

Hospira

PRINCIPAL DISPLAY PANEL -- 500 mL Bag Label -- IM-0096
(click image for full-size original)

PRINCIPAL DISPLAY PANEL — 500 mL Bag Label — IM-0065

10 mEq POTASSIUM

500 mL

NDC 0409-7902-03

10 mEq

POTASSIUM
CHLORIDE
in 5% Dextrose and
0.45% Sodium Chloride Inj., USP

EACH 100 mL CONTAINS POTASSIUM CHLORIDE 149 mg; SODIUM
CHLORIDE 450 mg; DEXTROSE, HYDROUS 5 g IN WATER
FOR INJECTION. MAY CONTAIN HCl FOR pH ADJUSTMENT.
ELECTROLYTES PER 1000 mL (NOT INCLUDING IONS FOR pH
ADJUSTMENT): POTASSIUM 20 mEq; SODIUM 77 mEq; CHLORIDE 97 mEq.

447 mOsmol/LITER (CALC.)
pH 4.2 (3.5 to 6.5)

ADDITIVES MAY BE INCOMPATIBLE. CONSULT WITH
PHARMACIST, IF AVAILABLE. WHEN INTRODUCING
ADDITIVES, USE ASEPTIC TECHNIQUE, MIX
THOROUGHLY AND DO NOT STORE.

SINGLE-DOSE CONTAINER. FOR I.V. USE. USUAL DOSAGE: SEE INSERT.
STERILE, NONPYROGENIC. USE ONLY IF SOLUTION IS CLEAR AND
CONTAINER IS UNDAMAGED. MUST NOT BE USED IN SERIES
CONNECTIONS.

Rx ONLY

3
v
CONTAINS DEHP

PRINTED IN USA
©HOSPIRA 2004
IM-0065 (4/04)HOSPIRA, INC., LAKE FOREST, IL 60045 USA

Hospira

PRINCIPAL DISPLAY PANEL -- 500 mL Bag Label -- IM-0065
(click image for full-size original)

PRINCIPAL DISPLAY PANEL — 1000 mL Bag Label — IM-0091

10 mEq POTASSIUM

1000 mL

NDC 0409-7997-09

10 mEq

POTASSIUM
CHLORIDE

in 5% Dextrose and
0.225% Sodium Chloride
Injection, USP

EACH 100 mL CONTAINS POTASSIUM
CHLORIDE 74.5 mg; SODIUM CHLORIDE 225 mg;
DEXTROSE, HYDROUS 5 g IN WATER FOR
INJECTION. MAY CONTAIN HCl FOR pH
ADJUSTMENT.

ELECTROLYTES PER 1000 mL (NOT INCLUDING
IONS FOR pH ADJUSTMENT): POTASSIUM
10 mEq; SODIUM 38.5 mEq; CHLORIDE 48.5 mEq.

349 mOsmol/LITER (CALC.)
pH 4.2 (3.5 to 6.5)

ADDITIVES MAY BE INCOMPATIBLE.
CONSULT WITH PHARMACIST, IF AVAILABLE.
WHEN INTRODUCING ADDITIVES,
USE ASEPTIC TECHNIQUE, MIX THOROUGHLY
AND DO NOT STORE.

SINGLE-DOSE CONTAINER. FOR I.V. USE.
USUAL DOSAGE: SEE INSERT. STERILE,
NONPYROGENIC. USE ONLY IF SOLUTION IS
CLEAR AND CONTAINER IS UNDAMAGED.
MUST NOT BE USED IN SERIES CONNECTIONS.

Rx ONLY

3
v
CONTAINS DEHP

PRINTED IN USA

©HOSPIRA 2004IM-0091 (4/04)

HOSPIRA, INC., LAKE FOREST, IL 60045 USA

Hospira

PRINCIPAL DISPLAY PANEL -- 1000 mL Bag Label -- IM-0091
(click image for full-size original)

PRINCIPAL DISPLAY PANEL — Overwrap

TO OPEN TEAR AT NOTCH

2 HDPE

DO NOT REMOVE FROM OVERWRAP UNTIL READY FOR USE. AFTER REMOVING
THE OVERWRAP, CHECK FOR MINUTE LEAKS BY SQUEEZING CONTAINER FIRMLY.
IF LEAKS ARE FOUND, DISCARD SOLUTION AS STERILITY MAY BE IMPAIRED.
RECOMMENDED STORAGE: ROOM TEMPERATURE (25°C). AVOID EXCESSIVE
HEAT. PROTECT FROM FREEZING. SEE INSERT.98-4321-R14-3/98

PRINCIPAL DISPLAY PANEL -- Overwrap
(click image for full-size original)
POTASSIUM CHLORIDE IN DEXTROSE AND SODIUM CHLORIDE dextrose monohydrate, sodium chloride, and potassium chloride injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0409-7107
Route of Administration INTRAVENOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DEXTROSE MONOHYDRATE (ANHYDROUS DEXTROSE) DEXTROSE MONOHYDRATE 50 g in 1000 mL
SODIUM CHLORIDE (SODIUM CATION and CHLORIDE ION) SODIUM CHLORIDE 9 g in 1000 mL
POTASSIUM CHLORIDE (POTASSIUM CATION and CHLORIDE ION) POTASSIUM CHLORIDE 1.49 g in 1000 mL
Inactive Ingredients
Ingredient Name Strength
WATER
HYDROCHLORIC ACID
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0409-7107-09 12 POUCH in 1 CASE contains a POUCH
1 1 BAG in 1 POUCH This package is contained within the CASE (0409-7107-09) and contains a BAG
1 1000 mL in 1 BAG This package is contained within a POUCH and a CASE (0409-7107-09)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA019691 12/31/2004 09/01/2020
POTASSIUM CHLORIDE IN DEXTROSE AND SODIUM CHLORIDE dextrose monohydrate, sodium chloride, and potassium chloride injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0409-7109
Route of Administration INTRAVENOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DEXTROSE MONOHYDRATE (ANHYDROUS DEXTROSE) DEXTROSE MONOHYDRATE 50 g in 1000 mL
SODIUM CHLORIDE (SODIUM CATION and CHLORIDE ION) SODIUM CHLORIDE 9 g in 1000 mL
POTASSIUM CHLORIDE (POTASSIUM CATION and CHLORIDE ION) POTASSIUM CHLORIDE 2.98 g in 1000 mL
Inactive Ingredients
Ingredient Name Strength
WATER
HYDROCHLORIC ACID
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0409-7109-09 12 POUCH in 1 CASE contains a POUCH
1 1 BAG in 1 POUCH This package is contained within the CASE (0409-7109-09) and contains a BAG
1 1000 mL in 1 BAG This package is contained within a POUCH and a CASE (0409-7109-09)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA019691 03/31/2005 05/01/2020
POTASSIUM CHLORIDE IN DEXTROSE AND SODIUM CHLORIDE dextrose monohydrate, sodium chloride, and potassium chloride injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0409-7903
Route of Administration INTRAVENOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DEXTROSE MONOHYDRATE (ANHYDROUS DEXTROSE) DEXTROSE MONOHYDRATE 50 g in 1000 mL
SODIUM CHLORIDE (SODIUM CATION and CHLORIDE ION) SODIUM CHLORIDE 4.5 g in 1000 mL
POTASSIUM CHLORIDE (POTASSIUM CATION and CHLORIDE ION) POTASSIUM CHLORIDE 2.24 g in 1000 mL
Inactive Ingredients
Ingredient Name Strength
WATER
HYDROCHLORIC ACID
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0409-7903-09 12 POUCH in 1 CASE contains a POUCH
1 1 BAG in 1 POUCH This package is contained within the CASE (0409-7903-09) and contains a BAG
1 1000 mL in 1 BAG This package is contained within a POUCH and a CASE (0409-7903-09)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA018362 11/01/2005 03/01/2021
POTASSIUM CHLORIDE IN DEXTROSE AND SODIUM CHLORIDE dextrose monohydrate, sodium chloride, and potassium chloride injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0409-7904
Route of Administration INTRAVENOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DEXTROSE MONOHYDRATE (ANHYDROUS DEXTROSE) DEXTROSE MONOHYDRATE 50 g in 1000 mL
SODIUM CHLORIDE (SODIUM CATION and CHLORIDE ION) SODIUM CHLORIDE 4.5 g in 1000 mL
POTASSIUM CHLORIDE (POTASSIUM CATION and CHLORIDE ION) POTASSIUM CHLORIDE 2.98 g in 1000 mL
Inactive Ingredients
Ingredient Name Strength
WATER
HYDROCHLORIC ACID
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0409-7904-09 12 POUCH in 1 CASE contains a POUCH
1 1 BAG in 1 POUCH This package is contained within the CASE (0409-7904-09) and contains a BAG
1 1000 mL in 1 BAG This package is contained within a POUCH and a CASE (0409-7904-09)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA018362 06/03/2005 08/01/2021
POTASSIUM CHLORIDE IN DEXTROSE AND SODIUM CHLORIDE dextrose monohydrate, sodium chloride, and potassium chloride injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0409-7991
Route of Administration INTRAVENOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DEXTROSE MONOHYDRATE (ANHYDROUS DEXTROSE) DEXTROSE MONOHYDRATE 50 g in 1000 mL
SODIUM CHLORIDE (SODIUM CATION and CHLORIDE ION) SODIUM CHLORIDE 2.25 g in 1000 mL
POTASSIUM CHLORIDE (POTASSIUM CATION and CHLORIDE ION) POTASSIUM CHLORIDE 2.24 g in 1000 mL
Inactive Ingredients
Ingredient Name Strength
WATER
HYDROCHLORIC ACID
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0409-7991-09 12 POUCH in 1 CASE contains a POUCH
1 1 BAG in 1 POUCH This package is contained within the CASE (0409-7991-09) and contains a BAG
1 1000 mL in 1 BAG This package is contained within a POUCH and a CASE (0409-7991-09)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA018365 09/29/2005 08/01/2010
POTASSIUM CHLORIDE IN DEXTROSE AND SODIUM CHLORIDE dextrose monohydrate, sodium chloride, and potassium chloride injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0409-7992
Route of Administration INTRAVENOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DEXTROSE MONOHYDRATE (ANHYDROUS DEXTROSE) DEXTROSE MONOHYDRATE 50 g in 1000 mL
SODIUM CHLORIDE (SODIUM CATION and CHLORIDE ION) SODIUM CHLORIDE 2.25 g in 1000 mL
POTASSIUM CHLORIDE (POTASSIUM CATION and CHLORIDE ION) POTASSIUM CHLORIDE 2.98 g in 1000 mL
Inactive Ingredients
Ingredient Name Strength
WATER
HYDROCHLORIC ACID
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0409-7992-09 12 POUCH in 1 CASE contains a POUCH
1 1 BAG in 1 POUCH This package is contained within the CASE (0409-7992-09) and contains a BAG
1 1000 mL in 1 BAG This package is contained within a POUCH and a CASE (0409-7992-09)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA018365 09/29/2005 03/01/2011
POTASSIUM CHLORIDE IN DEXTROSE AND SODIUM CHLORIDE dextrose monohydrate, sodium chloride, and potassium chloride injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0409-7993
Route of Administration INTRAVENOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DEXTROSE MONOHYDRATE (ANHYDROUS DEXTROSE) DEXTROSE MONOHYDRATE 50 g in 1000 mL
SODIUM CHLORIDE (SODIUM CATION and CHLORIDE ION) SODIUM CHLORIDE 4.5 g in 1000 mL
POTASSIUM CHLORIDE (POTASSIUM CATION and CHLORIDE ION) POTASSIUM CHLORIDE 0.745 g in 1000 mL
Inactive Ingredients
Ingredient Name Strength
WATER
HYDROCHLORIC ACID
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0409-7993-09 12 POUCH in 1 CASE contains a POUCH
1 1 BAG in 1 POUCH This package is contained within the CASE (0409-7993-09) and contains a BAG
1 1000 mL in 1 BAG This package is contained within a POUCH and a CASE (0409-7993-09)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA018362 02/28/2005 03/01/2021
POTASSIUM CHLORIDE IN DEXTROSE AND SODIUM CHLORIDE dextrose monohydrate, sodium chloride, and potassium chloride injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0409-7901
Route of Administration INTRAVENOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DEXTROSE MONOHYDRATE (ANHYDROUS DEXTROSE) DEXTROSE MONOHYDRATE 50 g in 1000 mL
SODIUM CHLORIDE (SODIUM CATION and CHLORIDE ION) SODIUM CHLORIDE 2.25 g in 1000 mL
POTASSIUM CHLORIDE (POTASSIUM CATION and CHLORIDE ION) POTASSIUM CHLORIDE 1.49 g in 1000 mL
Inactive Ingredients
Ingredient Name Strength
WATER
HYDROCHLORIC ACID
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0409-7901-03 24 POUCH in 1 CASE contains a POUCH
1 1 BAG in 1 POUCH This package is contained within the CASE (0409-7901-03) and contains a BAG
1 500 mL in 1 BAG This package is contained within a POUCH and a CASE (0409-7901-03)
2 NDC:0409-7901-09 12 POUCH in 1 CASE contains a POUCH
2 1 BAG in 1 POUCH This package is contained within the CASE (0409-7901-09) and contains a BAG
2 1000 mL in 1 BAG This package is contained within a POUCH and a CASE (0409-7901-09)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA018365 03/30/2005 07/08/2022
POTASSIUM CHLORIDE IN DEXTROSE AND SODIUM CHLORIDE dextrose monohydrate, sodium chloride, and potassium chloride injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0409-7998
Route of Administration INTRAVENOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DEXTROSE MONOHYDRATE (ANHYDROUS DEXTROSE) DEXTROSE MONOHYDRATE 50 g in 1000 mL
SODIUM CHLORIDE (SODIUM CATION and CHLORIDE ION) SODIUM CHLORIDE 3 g in 1000 mL
POTASSIUM CHLORIDE (POTASSIUM CATION and CHLORIDE ION) POTASSIUM CHLORIDE 1.49 g in 1000 mL
Inactive Ingredients
Ingredient Name Strength
WATER
HYDROCHLORIC ACID
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0409-7998-03 24 POUCH in 1 CASE contains a POUCH
1 1 BAG in 1 POUCH This package is contained within the CASE (0409-7998-03) and contains a BAG
1 500 mL in 1 BAG This package is contained within a POUCH and a CASE (0409-7998-03)
2 NDC:0409-7998-09 12 POUCH in 1 CASE contains a POUCH
2 1 BAG in 1 POUCH This package is contained within the CASE (0409-7998-09) and contains a BAG
2 1000 mL in 1 BAG This package is contained within a POUCH and a CASE (0409-7998-09)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA018876 02/28/2005 12/01/2010
POTASSIUM CHLORIDE IN DEXTROSE AND SODIUM CHLORIDE dextrose monohydrate, sodium chloride, and potassium chloride injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0409-7902
Route of Administration INTRAVENOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DEXTROSE MONOHYDRATE (ANHYDROUS DEXTROSE) DEXTROSE MONOHYDRATE 50 g in 1000 mL
SODIUM CHLORIDE (SODIUM CATION and CHLORIDE ION) SODIUM CHLORIDE 4.5 g in 1000 mL
POTASSIUM CHLORIDE (POTASSIUM CATION and CHLORIDE ION) POTASSIUM CHLORIDE 1.49 g in 1000 mL
Inactive Ingredients
Ingredient Name Strength
WATER
HYDROCHLORIC ACID
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0409-7902-03 24 POUCH in 1 CASE contains a POUCH
1 1 BAG in 1 POUCH This package is contained within the CASE (0409-7902-03) and contains a BAG
1 500 mL in 1 BAG This package is contained within a POUCH and a CASE (0409-7902-03)
2 NDC:0409-7902-09 12 POUCH in 1 CASE contains a POUCH
2 1 BAG in 1 POUCH This package is contained within the CASE (0409-7902-09) and contains a BAG
2 1000 mL in 1 BAG This package is contained within a POUCH and a CASE (0409-7902-09)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA018362 01/31/2005 08/01/2021
POTASSIUM CHLORIDE IN DEXTROSE AND SODIUM CHLORIDE dextrose monohydrate, sodium chloride, and potassium chloride injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0409-7997
Route of Administration INTRAVENOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DEXTROSE MONOHYDRATE (ANHYDROUS DEXTROSE) DEXTROSE MONOHYDRATE 50 g in 1000 mL
SODIUM CHLORIDE (SODIUM CATION and CHLORIDE ION) SODIUM CHLORIDE 2.25 g in 1000 mL
POTASSIUM CHLORIDE (POTASSIUM CATION and CHLORIDE ION) POTASSIUM CHLORIDE 0.745 g in 1000 mL
Inactive Ingredients
Ingredient Name Strength
WATER
HYDROCHLORIC ACID
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0409-7997-09 12 POUCH in 1 CASE contains a POUCH
1 1 BAG in 1 POUCH This package is contained within the CASE (0409-7997-09) and contains a BAG
1 1000 mL in 1 BAG This package is contained within a POUCH and a CASE (0409-7997-09)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA018365 01/31/2005 05/01/2010
Labeler — Hospira, Inc. (141588017)
Establishment
Name Address ID/FEI Operations
Hospira, Inc. 827731089 ANALYSIS (0409-7107), ANALYSIS (0409-7109), ANALYSIS (0409-7901), ANALYSIS (0409-7902), ANALYSIS (0409-7903), ANALYSIS (0409-7904), ANALYSIS (0409-7991), ANALYSIS (0409-7992), ANALYSIS (0409-7993), ANALYSIS (0409-7997), ANALYSIS (0409-7998)

Revised: 03/2017 Hospira, Inc.

Page 4 of 4 1 2 3 4

All MedLibrary.org resources are included in as near-original form as possible, meaning that the information from the original provider has been rendered here with only typographical or stylistic modifications and not with any substantive alterations of content, meaning or intent.

This site is provided for educational and informational purposes only, in accordance with our Terms of Use, and is not intended as a substitute for the advice of a medical doctor, nurse, nurse practitioner or other qualified health professional.

Privacy Policy | Copyright © 2022. All Rights Reserved.