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01 12care4
02 4Abbott Laboratories
03 3American Regent
04 2B. Braun Medical
05 1Fresenius Kabi AB Brunna
06 3Fresenius Kabi USA
07 3Hospira, Inc.
08 1ICU Medical
09 1Lukare medical
10 1Pharmachim Ab
11 2Recordati
12 1Vantive Belgium
13 2Vantive Belgium Srl
14 1Vantive Gmbh
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01 1Concentrate For Solution For Infusion
02 3Dialysis Solution
03 9INJECTABLE;INJECTION
04 1INJECTABLE;INTRATHECAL
05 3Oral Solution
06 7SOLUTION;INTRAVENOUS
07 1Solution
08 1Solution For Hemodialysis/Hemofiltration
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01 1Allowed
02 3Approved
03 2Authorized
04 8DISCN
05 3Deregistered
06 9RX
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01 1AMINOSYN II 3.5% M
02 3AMINOSYN II 3.5% M IN DEXTROSE 5% IN PLASTIC CONTAINER
03 1AMINOSYN II 3.5% M IN PLASTIC CONTAINER
04 2AMINOSYN II 4.25% M IN DEXTROSE 10% IN PLASTIC CONTAINER
05 1Addiphos
06 2Biphozyl
07 1ELLIOTTS B SOLUTION
08 2ISOLYTE S PH 7.4 IN PLASTIC CONTAINER
09 3Phosphoric
10 1Phosphosodine
11 2Phoxilium
12 6SODIUM PHOSPHATES
13 1SODIUM PHOSPHATES IN PLASTIC CONTAINER
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01 2Spain
02 6Sweden
03 1Switzerland
04 17USA
Regulatory Info : DISCN
Registration Country : USA
AMINO ACIDS; MAGNESIUM ACETATE; POTASSIUM ACETATE; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE
Brand Name : AMINOSYN II 3.5% M IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 3.5%;32MG/100ML;128MG/100ML;222MG/100ML;49MG/100ML
Packaging :
Approval Date : 1986-10-16
Application Number : 19493
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMINO ACIDS; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE
Brand Name : AMINOSYN II 3.5% M IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 3.5%;5GM/100ML;30MG/100ML;97MG/100ML;120MG/100ML;49.3MG/100ML
Packaging :
Approval Date : 1986-12-16
Application Number : 19564
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMINO ACIDS; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE
Brand Name : AMINOSYN II 4.25% M IN DEXTROSE 10% IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 4.25%;10GM/100ML;30MG/100ML;97MG/100ML;120MG/100ML;49.3MG/100ML
Packaging :
Approval Date : 1986-12-16
Application Number : 19564
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMINO ACIDS; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE
Brand Name : AMINOSYN II 3.5% M IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 3.5%;5GM/100ML;30MG/100ML;97MG/100ML;120MG/100ML;49.3MG/100ML
Packaging :
Approval Date : 1988-09-08
Application Number : 19712
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE
Brand Name : SODIUM PHOSPHATES
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : 1.34GM/5ML;1.38GM/5ML (268MG/ML;276MG/ML)
Packaging :
Approval Date : 2024-06-21
Application Number : 218314
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE
Brand Name : SODIUM PHOSPHATES
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : 4.02GM/15ML;4.14GM/15ML (268MG/ML;276MG/ML)
Packaging :
Approval Date : 2024-06-21
Application Number : 218314
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE
Brand Name : SODIUM PHOSPHATES
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : 13.4GM/50ML;13.8GM/50ML (268MG/ML;276MG/ML)
Packaging :
Approval Date : 2024-06-21
Application Number : 218314
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, MONOBASIC; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE
Brand Name : ISOLYTE S PH 7.4 IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 30MG/100ML;37MG/100ML;0.82MG/100ML;370MG/100ML;530MG/100ML;500MG/100ML;12MG/100ML
Packaging :
Approval Date : 1984-04-04
Application Number : 19006
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, MONOBASIC; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE
Brand Name : ISOLYTE S PH 7.4 IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 30MG/100ML;37MG/100ML;0.82MG/100ML;370MG/100ML;530MG/100ML;500MG/100ML;12MG/100ML
Packaging :
Approval Date : 1989-09-29
Application Number : 19696
Regulatory Info : RX
Registration Country : USA
Regulatory Info : Deregistered
Registration Country : Sweden
Disodium Phosphate Dihydrate; Calcium Chloride Dihydrate; Potassium Chloride; Magnesium Chloride Hexahydrate; Sodium Chloride; Sodium Bicarbonate
Brand Name : Addiphos
Dosage Form : Concentrate For Solution For Infusion
Dosage Strength :
Packaging :
Approval Date : 07/12/1984
Application Number : 19841207000039
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : RX
Registration Country : USA
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE
Brand Name : SODIUM PHOSPHATES
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : 1.34GM/5ML;1.38GM/5ML (268MG/ML;276MG/ML)
Packaging :
Approval Date : 2022-03-30
Application Number : 209997
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE
Brand Name : SODIUM PHOSPHATES
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : 4.02GM/15ML;4.14GM/15ML (268MG/ML;276MG/ML)
Packaging :
Approval Date : 2022-03-30
Application Number : 209997
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE
Brand Name : SODIUM PHOSPHATES
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : 13.4GM/50ML;13.8GM/50ML (268MG/ML;276MG/ML)
Packaging :
Approval Date : 2022-03-30
Application Number : 209997
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE
Brand Name : SODIUM PHOSPHATES IN PLASTIC CONTAINER
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : 4.02GM/15ML;4.14GM/15ML (268MG/ML;276MG/ML)
Packaging :
Approval Date : 1983-05-10
Application Number : 18892
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMINO ACIDS; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE
Brand Name : AMINOSYN II 3.5% M IN DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 3.5%;5GM/100ML;30MG/100ML;97MG/100ML;120MG/100ML;49.3MG/100ML
Packaging :
Approval Date : 1988-11-01
Application Number : 19682
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMINO ACIDS; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE
Brand Name : AMINOSYN II 4.25% M IN DEXTROSE 10% IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 4.25%;5GM/100ML;30MG/100ML;97MG/100ML;120MG/100ML;49.3MG/100ML
Packaging :
Approval Date : 1988-11-01
Application Number : 19682
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMINO ACIDS; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE
Brand Name : AMINOSYN II 3.5% M
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 3.5%;30MG/100ML;97MG/100ML;120MG/100ML;49MG/100ML
Packaging :
Approval Date : 1986-04-03
Application Number : 19437
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM SULFATE; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE
Brand Name : ELLIOTTS B SOLUTION
Dosage Form : INJECTABLE;INTRATHECAL
Dosage Strength : 0.2MG/ML;0.8MG/ML;0.3MG/ML;0.3MG/ML;1.9MG/ML;7.3MG/ML;0.2MG/ML
Packaging :
Approval Date : 1996-09-27
Application Number : 20577
Regulatory Info : RX
Registration Country : USA
Regulatory Info : Approved
Registration Country : Sweden
Disodium Phosphate Dihydrate; Calcium Chloride Dihydrate; Potassium Chloride; Magnesium Chloride Hexahydrate; Sodium Chloride; Sodium Bicarbonate
Brand Name : Phoxilium
Dosage Form : Dialysis Solution
Dosage Strength : 1.2mmol/lphosphate
Packaging :
Approval Date : 23/10/2009
Application Number : 20080212000016
Regulatory Info : Approved
Registration Country : Sweden
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : Approved
Registration Country : Sweden
Disodium Phosphate Dihydrate; Calcium Chloride Dihydrate; Potassium Chloride; Magnesium Chloride Hexahydrate; Sodium Chloride; Sodium Bicarbonate
Brand Name : Biphozyl
Dosage Form : Dialysis Solution
Dosage Strength :
Packaging :
Approval Date : 12/12/2014
Application Number : 20130918000015
Regulatory Info : Approved
Registration Country : Sweden
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF