Reviews Theophylline in 5% Dextrose Injection Excel Container


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Theophylline in 5% Dextrose Injection Excel Container Drug Description
Theophylline in 5% Dextrose Injections USP
Excel Container
Do not admix with other drugs.
DRUG DESCRIPTION
Theophylline in 5% Dextrose Injections USP are sterile, nonpyrogenic solutions
intended for intravenous administration, prepared from theophylline and dextrose
in Water for Injection USP.
Composition - Each 100 mL contains



Solution
Anhydrous Theophylline USP
Hydrous Dextrose USP
pH
Calculated Osmolarity mOsmol/liter


0.08% Theophylline in 5% Dextrose Injection USP
80 mg
5 g
4.7 (3.5-6.5)
255


0.16% Theophylline in 5% Dextrose Injection USP
160 mg
5 g
4.7 (3.5-6.5)
260



Water for Injection USP, qs
Theophylline is structurally classified as a methylxanthine. It occurs as a
white, odorless, crystalline powder with a bitter taste. Anhydrous theophylline
has the chemical name 1H-Purine-2, 6-dione, 3,7-dihydro-1, 3-dimethyl-, and
is represented by the following structural formula:
The formulas of the active ingredients are:







Theophylline, Anhydrous, USP







Hydrous Dextrose USP
The molecular formula of anhydrous theophylline is C7H8N4O2
with a molecular weight of 180.17. The molecular formula of hydrous dextrose
is C6H12O6•H2O with a molecular
weight of 198.17.
The EXCEL Container is Latex-free; PVC-free; and DEHP-free.
The plastic container is made from a multilayered film specifically developed
for parenteral drugs. It contains no plasticizers and exhibits virtually no
leachables. The solution contact layer is a rubberized copolymer of ethylene
and propylene. The container is nontoxic and biologically inert. The container-solution
unit is a closed system and is not dependent upon entry of external air during
administration. The container is overwrapped to provide protection from the
physical environment and to provide an additional moisture barrier when necessary.
The closure system has two ports; the one for the administration set has a
tamper evident plastic protector. Refer to the Directions for Use of the container.Last reviewed on RxList: 8/28/2008




Theophylline in 5% Dextrose Injection Excel Container Drug Description
Theophylline in 5% Dextrose Injections USP
Excel Container
Do not admix with other drugs.
DRUG DESCRIPTION
Theophylline in 5% Dextrose Injections USP are sterile, nonpyrogenic solutions
intended for intravenous administration, prepared from theophylline and dextrose
in Water for Injection USP.
Composition - Each 100 mL contains



Solution
Anhydrous Theophylline USP
Hydrous Dextrose USP
pH
Calculated Osmolarity mOsmol/liter


0.08% Theophylline in 5% Dextrose Injection USP
80 mg
5 g
4.7 (3.5-6.5)
255


0.16% Theophylline in 5% Dextrose Injection USP
160 mg
5 g
4.7 (3.5-6.5)
260



Water for Injection USP, qs
Theophylline is structurally classified as a methylxanthine. It occurs as a
white, odorless, crystalline powder with a bitter taste. Anhydrous theophylline
has the chemical name 1H-Purine-2, 6-dione, 3,7-dihydro-1, 3-dimethyl-, and
is represented by the following structural formula:
The formulas of the active ingredients are:







Theophylline, Anhydrous, USP







Hydrous Dextrose USP
The molecular formula of anhydrous theophylline is C7H8N4O2
with a molecular weight of 180.17. The molecular formula of hydrous dextrose
is C6H12O6•H2O with a molecular
weight of 198.17.
The EXCEL Container is Latex-free; PVC-free; and DEHP-free.
The plastic container is made from a multilayered film specifically developed
for parenteral drugs. It contains no plasticizers and exhibits virtually no
leachables. The solution contact layer is a rubberized copolymer of ethylene
and propylene. The container is nontoxic and biologically inert. The container-solution
unit is a closed system and is not dependent upon entry of external air during
administration. The container is overwrapped to provide protection from the
physical environment and to provide an additional moisture barrier when necessary.
The closure system has two ports; the one for the administration set has a
tamper evident plastic protector. Refer to the Directions for Use of the container.Last reviewed on RxList: 8/28/2008




Theophylline in 5% Dextrose Injection Excel Container Drug Description
Theophylline in 5% Dextrose Injections USP
Excel Container
Do not admix with other drugs.
DRUG DESCRIPTION
Theophylline in 5% Dextrose Injections USP are sterile, nonpyrogenic solutions
intended for intravenous administration, prepared from theophylline and dextrose
in Water for Injection USP.
Composition - Each 100 mL contains



Solution
Anhydrous Theophylline USP
Hydrous Dextrose USP
pH
Calculated Osmolarity mOsmol/liter


0.08% Theophylline in 5% Dextrose Injection USP
80 mg
5 g
4.7 (3.5-6.5)
255


0.16% Theophylline in 5% Dextrose Injection USP
160 mg
5 g
4.7 (3.5-6.5)
260



Water for Injection USP, qs
Theophylline is structurally classified as a methylxanthine. It occurs as a
white, odorless, crystalline powder with a bitter taste. Anhydrous theophylline
has the chemical name 1H-Purine-2, 6-dione, 3,7-dihydro-1, 3-dimethyl-, and
is represented by the following structural formula:
The formulas of the active ingredients are:







Theophylline, Anhydrous, USP







Hydrous Dextrose USP
The molecular formula of anhydrous theophylline is C7H8N4O2
with a molecular weight of 180.17. The molecular formula of hydrous dextrose
is C6H12O6•H2O with a molecular
weight of 198.17.
The EXCEL Container is Latex-free; PVC-free; and DEHP-free.
The plastic container is made from a multilayered film specifically developed
for parenteral drugs. It contains no plasticizers and exhibits virtually no
leachables. The solution contact layer is a rubberized copolymer of ethylene
and propylene. The container is nontoxic and biologically inert. The container-solution
unit is a closed system and is not dependent upon entry of external air during
administration. The container is overwrapped to provide protection from the
physical environment and to provide an additional moisture barrier when necessary.
The closure system has two ports; the one for the administration set has a
tamper evident plastic protector. Refer to the Directions for Use of the container.Last reviewed on RxList: 8/28/2008




Theophylline in 5% Dextrose Injection Excel Container Drug Description
Theophylline in 5% Dextrose Injections USP
Excel Container
Do not admix with other drugs.
DRUG DESCRIPTION
Theophylline in 5% Dextrose Injections USP are sterile, nonpyrogenic solutions
intended for intravenous administration, prepared from theophylline and dextrose
in Water for Injection USP.
Composition - Each 100 mL contains



Solution
Anhydrous Theophylline USP
Hydrous Dextrose USP
pH
Calculated Osmolarity mOsmol/liter


0.08% Theophylline in 5% Dextrose Injection USP
80 mg
5 g
4.7 (3.5-6.5)
255


0.16% Theophylline in 5% Dextrose Injection USP
160 mg
5 g
4.7 (3.5-6.5)
260



Water for Injection USP, qs
Theophylline is structurally classified as a methylxanthine. It occurs as a
white, odorless, crystalline powder with a bitter taste. Anhydrous theophylline
has the chemical name 1H-Purine-2, 6-dione, 3,7-dihydro-1, 3-dimethyl-, and
is represented by the following structural formula:
The formulas of the active ingredients are:







Theophylline, Anhydrous, USP







Hydrous Dextrose USP
The molecular formula of anhydrous theophylline is C7H8N4O2
with a molecular weight of 180.17. The molecular formula of hydrous dextrose
is C6H12O6•H2O with a molecular
weight of 198.17.
The EXCEL Container is Latex-free; PVC-free; and DEHP-free.
The plastic container is made from a multilayered film specifically developed
for parenteral drugs. It contains no plasticizers and exhibits virtually no
leachables. The solution contact layer is a rubberized copolymer of ethylene
and propylene. The container is nontoxic and biologically inert. The container-solution
unit is a closed system and is not dependent upon entry of external air during
administration. The container is overwrapped to provide protection from the
physical environment and to provide an additional moisture barrier when necessary.
The closure system has two ports; the one for the administration set has a
tamper evident plastic protector. Refer to the Directions for Use of the container.Last reviewed on RxList: 8/28/2008




Theophylline in 5% Dextrose Injection Excel Container Drug Description
Theophylline in 5% Dextrose Injections USP
Excel Container
Do not admix with other drugs.
DRUG DESCRIPTION
Theophylline in 5% Dextrose Injections USP are sterile, nonpyrogenic solutions
intended for intravenous administration, prepared from theophylline and dextrose
in Water for Injection USP.
Composition - Each 100 mL contains



Solution
Anhydrous Theophylline USP
Hydrous Dextrose USP
pH
Calculated Osmolarity mOsmol/liter


0.08% Theophylline in 5% Dextrose Injection USP
80 mg
5 g
4.7 (3.5-6.5)
255


0.16% Theophylline in 5% Dextrose Injection USP
160 mg
5 g
4.7 (3.5-6.5)
260



Water for Injection USP, qs
Theophylline is structurally classified as a methylxanthine. It occurs as a
white, odorless, crystalline powder with a bitter taste. Anhydrous theophylline
has the chemical name 1H-Purine-2, 6-dione, 3,7-dihydro-1, 3-dimethyl-, and
is represented by the following structural formula:
The formulas of the active ingredients are:







Theophylline, Anhydrous, USP







Hydrous Dextrose USP
The molecular formula of anhydrous theophylline is C7H8N4O2
with a molecular weight of 180.17. The molecular formula of hydrous dextrose
is C6H12O6•H2O with a molecular
weight of 198.17.
The EXCEL Container is Latex-free; PVC-free; and DEHP-free.
The plastic container is made from a multilayered film specifically developed
for parenteral drugs. It contains no plasticizers and exhibits virtually no
leachables. The solution contact layer is a rubberized copolymer of ethylene
and propylene. The container is nontoxic and biologically inert. The container-solution
unit is a closed system and is not dependent upon entry of external air during
administration. The container is overwrapped to provide protection from the
physical environment and to provide an additional moisture barrier when necessary.
The closure system has two ports; the one for the administration set has a
tamper evident plastic protector. Refer to the Directions for Use of the container.Last reviewed on RxList: 8/28/2008





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Other reviews about Theophylline in 5% Dextrose Injection Excel Container on web:

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Theophylline in 5% Dextrose Injections USP are indicated as an ... Theophylline in 5% Dextrose Injections USP are supplied sterile and nonpyrogenic in EXCEL ® Containers. Theophylline Injection - Indications and Dosage


-----THEOPHYLLINE IN DEXTROSE -theophylline injection, solution Hospira, Inc. THEOPHYLLINE 200, 400 AND 800 mg in 5% Dextrose Injection, USP Flexible Plastic Container Do not admix with ... Theophylline in 5% Dextrose Injection


Theophylline in 5% Dextrose injection, USP, Flexible Plastic Container March 2009 Detailed View: Safety Labeling Changes Approved By FDA Center for Drug Evaluation and Research ... Theophylline in 5% Dextrose injection, USP, Flexible Plastic ...


Theophylline In 5% Dextrose Injection, USP. In VIAFLEX container (Baxter) Premix medications are exempt from minimum order charge. Cardinal Health:Theophylline In 5% Dextrose Injection, USP


Theophylline in 5% Dextrose Injections USP are sterile, nonpyrogenic solutions intended for ... The EXCEL Container is Latex-free; PVC-free; and DEHP-free. The plastic ... Theophylline Injection - Description and Clinical Pharmacology


Theophylline in 5% Dextrose Injection Excel Container: Theophylline in Dextrose Excel Container: Theophylline in 5% Dextrose Injection Flexible Plastic Container Vademecum de Argentina - Vademecum USA 2009 - T


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