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01 12care4

02 4Abbott Laboratories

03 3American Regent

04 1Amgros I/S

05 2B. Braun Medical

06 2Baxter Healthcare Corporation

07 3Fresenius Kabi AB Brunna

08 3Fresenius Kabi USA

09 3Hospira, Inc.

10 1ICU Medical

11 1Lukare medical

12 1Pharmachim Ab

13 3Recordati

14 1Vantive Belgium

15 3Vantive Belgium SRL

16 4Vantive Belgium Srl

17 1Vantive Gmbh

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PharmaCompass

01

ESF Europe
Not Confirmed
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ESF Europe
Not Confirmed

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

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02

ESF Europe
Not Confirmed
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ESF Europe
Not Confirmed

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

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03

ESF Europe
Not Confirmed
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ESF Europe
Not Confirmed

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

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04

ESF Europe
Not Confirmed
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ESF Europe
Not Confirmed

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

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05

ESF Europe
Not Confirmed
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ESF Europe
Not Confirmed

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

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06

ESF Europe
Not Confirmed
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ESF Europe
Not Confirmed

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

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07

ESF Europe
Not Confirmed
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ESF Europe
Not Confirmed

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

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08

ESF Europe
Not Confirmed
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ESF Europe
Not Confirmed

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

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09

ESF Europe
Not Confirmed
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ESF Europe
Not Confirmed

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

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10

ESF Europe
Not Confirmed
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ESF Europe
Not Confirmed

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

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11

ESF Europe
Not Confirmed
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ESF Europe
Not Confirmed

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

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12

ESF Europe
Not Confirmed
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ESF Europe
Not Confirmed

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

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13

ESF Europe
Not Confirmed
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ESF Europe
Not Confirmed

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

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14

ESF Europe
Not Confirmed
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ESF Europe
Not Confirmed

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

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15

ESF Europe
Not Confirmed
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ESF Europe
Not Confirmed

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

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16

ESF Europe
Not Confirmed
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ESF Europe
Not Confirmed

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

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17

ESF Europe
Not Confirmed
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ESF Europe
Not Confirmed

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

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18

Vantive Gmbh

Country
ESF Europe
Not Confirmed
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Vantive Gmbh

Country
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ESF Europe
Not Confirmed

Magnesium Chloride Hexahydrate; Sodium Chloride; Sodium Bicarbonate; Potassium Chloride; Disodium Phosphate Dihydrate; Sodium; Potassium; Magnesium; Chloride; Hydrogen Phosphate; Bicarbonate

Brand Name : Biphozyl

Dosage Form : Dialysis Solution

Dosage Strength :

Packaging :

Approval Date : 06/04/2017

Application Number : 66074

Regulatory Info : Allowed

Registration Country : Switzerland

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19

Vantive Belgium SRL

Country
ESF Europe
Not Confirmed
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Vantive Belgium SRL

Country
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ESF Europe
Not Confirmed

Disodium Phosphate Dihydrate; Magnesium Chloride Hexahydrate; Sodium Chloride; Sodium Hydrogen Carbonate; Potassium Chloride

Brand Name : Biphozyl

Dosage Form : Solution for Haemodialysis

Dosage Strength : 0.187G/L; 3.05G/L; 7.01G/L; 2.12G/L; 0.314G/L

Packaging :

Approval Date : 2015-02-19

Application Number :

Regulatory Info : Authorised

Registration Country : Malta

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20

Vantive Belgium SRL

Country
ESF Europe
Not Confirmed
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Vantive Belgium SRL

Country
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ESF Europe
Not Confirmed

Calcium chloride dihydrate; Disodium phosphate dihydrate; Magnesium Chloride Hexahydrate; Sodium chloride; Sodium bicarbonate; Potassium chloride

Brand Name : Phoxilium 1.2 mmol/l phosphate

Dosage Form : Hemodialysis Solution

Dosage Strength :

Packaging :

Approval Date :

Application Number :

Regulatory Info : Marketed

Registration Country : Norway

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