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01 4Abbott Laboratories

02 3American Regent

03 2B. Braun Medical

04 3Fresenius Kabi USA

05 3Hospira, Inc.

06 1ICU Medical

07 1Lukare medical

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PharmaCompass

01

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
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

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
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

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
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

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
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

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
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

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
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

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
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

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
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

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
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

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
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

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
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

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
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

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
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

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
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

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
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

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
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

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
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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