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01 2Taro Pharmaceutical Industries

02 4Abbott Laboratories

03 1Alberta Veterinary Laboratories

04 15B. Braun Medical

05 4BIEFFE MEDITAL SpA

06 1BIMEDA-MTC ANIMAL HEALTH INC

07 1BIO AGRI MIX LP

08 2Baxter Healthcare Corporation

09 3CAN-VET ANIMAL HEALTH SUPPLIES LTD.

10 2Exela Pharma Sciences, LLC.

11 1Fresenius Kabi AB Brunna

12 30Galenica MA

13 3Hospira, Inc.

14 1Huvepharma

15 3ICU Medical

16 4MONICO SpA

17 2Novartis Pharmaceuticals Corporation

18 1Omega Laboratories Limited

19 1PROFESSIONAL VETERINARY LABORATORIES

20 18SALF SpA

21 1Teva Pharmaceutical Industries

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PharmaCompass

01

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Fi Europe 2024
Not Confirmed

NEOMYCIN (NEOMYCIN SULFATE)

Brand Name : VIADERM KC CRM

Dosage Form : CREAM

Dosage Strength : 2.5MG/G

Packaging : 15/30/60/454GM

Approval Date :

Application Number : 717002

Regulatory Info : Prescription

Registration Country : Canada

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02

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Fi Europe 2024
Not Confirmed

NEOMYCIN (NEOMYCIN SULFATE)

Brand Name : VIADERM KC ONT

Dosage Form : OINTMENT

Dosage Strength : 2.5MG/G

Packaging : 15/30/400GM

Approval Date :

Application Number : 717029

Regulatory Info : Prescription

Registration Country : Canada

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03

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

AMINO ACIDS; MAGNESIUM ACETATE; PHOSPHORIC ACID; POTASSIUM ACETATE; SODIUM CHLORIDE

Brand Name : AMINOSYN 3.5% M IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 3.5%;21MG/100ML;40MG/100ML;128MG/100ML;234MG/100ML

Packaging :

Approval Date : 1984-05-15

Application Number : 18804

Regulatory Info : DISCN

Registration Country : USA

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04

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

AMINO ACIDS; MAGNESIUM ACETATE; PHOSPHORIC ACID; POTASSIUM ACETATE; SODIUM CHLORIDE

Brand Name : AMINOSYN 3.5% M IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 3.5%;21MG/100ML;40MG/100ML;128MG/100ML;234MG/100ML

Packaging :

Approval Date : 1984-08-08

Application Number : 18875

Regulatory Info : DISCN

Registration Country : USA

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05

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
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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06

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

AMINO ACIDS; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM ACETATE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM CHLORIDE

Brand Name : AMINOSYN II 4.25% W/ ELECT AND ADJUSTED PHOSPHATE IN DEXTROSE 10% IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 4.25%;10GM/100ML;51MG/100ML;176.5MG/100ML;22.4MG/100ML;104.5MG/100ML;205MG/100ML

Packaging :

Approval Date : 1988-09-08

Application Number : 19712

Regulatory Info : DISCN

Registration Country : USA

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07

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

AMINO ACIDS; MAGNESIUM ACETATE; PHOSPHORIC ACID; POTASSIUM ACETATE; POTASSIUM CHLORIDE; SODIUM ACETATE

Brand Name : FREAMINE III 8.5% W/ ELECTROLYTES

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 8.5%;110MG/100ML;230MG/100ML;10MG/100ML;440MG/100ML;690MG/100ML

Packaging :

Approval Date : 1988-07-01

Application Number : 16822

Regulatory Info : DISCN

Registration Country : USA

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08

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

DEXTROSE; MAGNESIUM ACETATE TETRAHYDRATE; POTASSIUM ACETATE; SODIUM CHLORIDE

Brand Name : PLASMA-LYTE 56 AND DEXTROSE 5% IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 5GM/100ML;32MG/100ML;128MG/100ML;234MG/100ML

Packaging :

Approval Date : 1982-01-01

Application Number : 17385

Regulatory Info : DISCN

Registration Country : USA

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09

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

MAGNESIUM ACETATE TETRAHYDRATE; POTASSIUM ACETATE; SODIUM CHLORIDE

Brand Name : PLASMA-LYTE 56 IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 32MG/100ML;128MG/100ML;234MG/100ML

Packaging :

Approval Date : 1984-06-15

Application Number : 19047

Regulatory Info : DISCN

Registration Country : USA

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10

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

POTASSIUM ACETATE

Brand Name : POTASSIUM ACETATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 2MEQ/ML

Packaging :

Approval Date : 2015-12-29

Application Number : 206203

Regulatory Info : RX

Registration Country : USA

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11

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

POTASSIUM ACETATE

Brand Name : POTASSIUM ACETATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 2MEQ/ML

Packaging :

Approval Date : 2021-10-20

Application Number : 212692

Regulatory Info : RX

Registration Country : USA

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12

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

Potassium Acetate

Brand Name : Potassium Acetate

Dosage Form :

Dosage Strength : 5 Ampoules Ev 3 Meq/Ml 10 Ml  

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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13

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

Sodium Chloride; Potassium Acetate; Magnesium Acetate

Brand Name : Balanced Electrolytic Of Maintenance

Dosage Form :

Dosage Strength : 1 500 Ml Bottle  

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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14

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

Sodium Chloride; Potassium Acetate; Magnesium Acetate

Brand Name : Balanced Electrolytic Of Maintenance

Dosage Form :

Dosage Strength : 1 Bottle 1,000 Ml  

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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15

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

Sodium Chloride; Potassium Acetate; Magnesium Acetate

Brand Name : Balanced Electrolytic Of Maintenance

Dosage Form :

Dosage Strength : 1 Bag 1,000 Ml  

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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16

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

Sodium Chloride; Potassium Acetate; Magnesium Acetate

Brand Name : Balanced Electrolytic Of Maintenance

Dosage Form :

Dosage Strength : 1 Bag 500 Ml  

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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Fi Europe 2024
Not Confirmed
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Fi Europe 2024
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Sodium Chloride; Potassium Acetate; Magnesium Acetate

Brand Name : Balanced Electrolytic Of Maintenance

Dosage Form :

Dosage Strength : 1 Bottle 250 Ml  

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

Sodium Chloride; Potassium Acetate; Magnesium Acetate

Brand Name : Balanced Electrolytic Of Maintenance

Dosage Form :

Dosage Strength : 1 Bag 250 Ml  

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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19

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

Sodium Chloride; Potassium Acetate; Magnesium Acetate

Brand Name : Balanced Electrolytic Of Maintenance

Dosage Form :

Dosage Strength : 1 Bottle 100 Ml  

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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20

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

Sodium Chloride; Potassium Acetate; Magnesium Acetate

Brand Name : Balanced Electrolytic Of Maintenance

Dosage Form :

Dosage Strength : 1 Bag 100 Ml  

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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21

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

Sodium Chloride; Potassium Acetate; Magnesium Acetate

Brand Name : Balanced Electrolytic Of Maintaining Ii

Dosage Form :

Dosage Strength : 1 Bottle 1,000  

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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22

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

AMINO ACIDS; MAGNESIUM CHLORIDE; POTASSIUM ACETATE; POTASSIUM CHLORIDE; SODIUM ACETATE

Brand Name : VEINAMINE 8%

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 8%;61MG/100ML;211MG/100ML;56MG/100ML;388MG/100ML

Packaging :

Approval Date : 1982-01-01

Application Number : 17957

Regulatory Info : DISCN

Registration Country : USA

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23

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

POTASSIUM ACETATE

Brand Name : POTASSIUM ACETATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 2MEQ/ML

Packaging :

Approval Date : 1984-07-20

Application Number : 18896

Regulatory Info : RX

Registration Country : USA

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24

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

AMINO ACIDS; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM ACETATE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM CHLORIDE

Brand Name : AMINOSYN II 4.25% W/ ELECT AND ADJUSTED PHOSPHATE IN DEXTROSE 10% IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 4.25%;10GM/100ML;51MG/100ML;176.5MG/100ML;22.4MG/100ML;104.5MG/100ML;205MG/100ML

Packaging :

Approval Date : 1988-11-01

Application Number : 19682

Regulatory Info : DISCN

Registration Country : USA

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Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

DEXTROSE; MAGNESIUM ACETATE; POTASSIUM ACETATE; SODIUM CHLORIDE

Brand Name : NORMOSOL-M AND DEXTROSE 5% IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 5GM/100ML;21MG/100ML;128MG/100ML;234MG/100ML

Packaging :

Approval Date : 1982-01-01

Application Number : 17610

Regulatory Info : RX

Registration Country : USA

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Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

AMINO ACIDS; MAGNESIUM ACETATE; PHOSPHORIC ACID; POTASSIUM ACETATE; SODIUM CHLORIDE

Brand Name : AMINOSYN 3.5% M

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 3.5%;21MG/100ML;40MG/100ML;128MG/100ML;234MG/100ML

Packaging :

Approval Date : 1982-01-01

Application Number : 17789

Regulatory Info : DISCN

Registration Country : USA

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Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

AMINO ACIDS; MAGNESIUM ACETATE; POTASSIUM ACETATE; SODIUM CHLORIDE

Brand Name : AMINOSYN 3.5% M

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 3.5%;21MG/100ML;128MG/100ML;234MG/100ML

Packaging :

Approval Date : 1982-01-01

Application Number : 17789

Regulatory Info : DISCN

Registration Country : USA

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MONICO SpA

Country
Fi Europe 2024
Not Confirmed
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MONICO SpA

Country
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Fi Europe 2024
Not Confirmed

Potassium Acetate

Brand Name : Potassium Acetate

Dosage Form :

Dosage Strength : 10 Vials Ev 3 Meq/Ml 10 Ml  

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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29

SALF SpA

Country
Fi Europe 2024
Not Confirmed
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SALF SpA

Country
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Fi Europe 2024
Not Confirmed

Potassium Acetate

Brand Name : Potassium Acetate

Dosage Form :

Dosage Strength : 5 Ampoules Ev 3 Meq/Ml 10 Ml  

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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SALF SpA

Country
Fi Europe 2024
Not Confirmed
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SALF SpA

Country
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Fi Europe 2024
Not Confirmed

Potassium Acetate

Brand Name : Potassium Acetate

Dosage Form :

Dosage Strength : 1 Bottle 3 Meq/Ml 30 Ml  

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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