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01 2Abbott Laboratories

02 27Adcock Ingram

03 2Alberta Veterinary Laboratories

04 1Alcon Inc

05 43B. Braun Medical

06 1B. Braun Melsungen AG

07 4B.BRAUN MILANO SpA

08 14BIEFFE MEDITAL SpA

09 38Baxter Healthcare Corporation

10 1Bayer AG

11 1CAN-VET ANIMAL HEALTH SUPPLIES LTD.

12 5CHIEF MEDICAL SUPPLIES LTD

13 3DOMINION VETERINARY LABORATORIES LTD.

14 4EUROSPITAL SpA

15 1Epic Pharma. LLC.

16 2Fresenius Kabi Austria

17 10Fresenius Kabi USA

18 5Fresenius SE & Co. KGaA

19 58Galenica MA

20 3Hikma Pharmaceuticals

21 7Hospira, Inc.

22 4ICU Medical

23 12MONICO SpA

24 2Matrix Environmental Solutions

25 4Milla Pharmaceuticals

26 1Omega Laboratories Limited

27 1Pfizer Inc

28 65SALF SpA

29 4VETOQUINOL N A INC

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PharmaCompass

01

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

SODIUM ACETATE

Brand Name : AMO ENDOSOL SOLUTION

Dosage Form : SOLUTION

Dosage Strength : 0.39%

Packaging : 500ML

Approval Date :

Application Number : 2007967

Regulatory Info : Ethical

Registration Country : Canada

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02

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

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

Brand Name : FREAMINE III 3% W/ ELECTROLYTES

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 3%;54MG/100ML;40MG/100ML;150MG/100ML;200MG/100ML;120MG/100ML

Packaging :

Approval Date : 1982-01-01

Application Number : 16822

Regulatory Info : DISCN

Registration Country : USA

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03

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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04

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE

Brand Name : ISOLYTE S IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 30MG/100ML;37MG/100ML;370MG/100ML;530MG/100ML;500MG/100ML

Packaging :

Approval Date : 1982-01-01

Application Number : 18252

Regulatory Info : DISCN

Registration Country : USA

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05

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

SODIUM ACETATE

Brand Name : ISOLYTE S PH 7.4 (MULTI-ELECTROLYTE INJECTION)

Dosage Form : SOLUTION

Dosage Strength : 370MG/100ML

Packaging : 500ML

Approval Date :

Application Number : 1931679

Regulatory Info : Ethical

Registration Country : Canada

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06

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

SODIUM ACETATE

Brand Name : ISOLYTE S (MULTI-ELECTROLYTE INJECTION)

Dosage Form : SOLUTION

Dosage Strength : 370MG/100ML

Packaging : 1000

Approval Date :

Application Number : 1931628

Regulatory Info : Ethical

Registration Country : Canada

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07

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE

Brand Name : PLASMA-LYTE 148 IN WATER IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 30MG/100ML;37MG/100ML;368MG/100ML;526MG/100ML;502MG/100ML

Packaging :

Approval Date : 1982-01-01

Application Number : 17378

Regulatory Info : RX

Registration Country : USA

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08

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE

Brand Name : PLASMA-LYTE A IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 30MG/100ML;37MG/100ML;368MG/100ML;526MG/100ML;502MG/100ML

Packaging :

Approval Date : 1982-11-22

Application Number : 17378

Regulatory Info : RX

Registration Country : USA

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09

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM LACTATE

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

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 37MG/100ML;5GM/100ML;30MG/100ML;119MG/100ML;161MG/100ML;94MG/100ML;138MG/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 17390

Regulatory Info : DISCN

Registration Country : USA

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10

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CALCIUM CHLORIDE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM LACTATE

Brand Name : PLASMA-LYTE R IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 36.8MG/100ML;30.5MG/100ML;74.6MG/100ML;640MG/100ML;496MG/100ML;89.6MG/100ML

Packaging :

Approval Date : 1982-01-01

Application Number : 17438

Regulatory Info : DISCN

Registration Country : USA

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11

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE

Brand Name : PLASMA-LYTE 148 AND DEXTROSE 5% IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 5GM/100ML;30MG/100ML;37MG/100ML;368MG/100ML;526MG/100ML;502MG/100ML

Packaging :

Approval Date : 1982-01-01

Application Number : 17451

Regulatory Info : DISCN

Registration Country : USA

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12

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

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

Brand Name : TRAVASOL 5.5% W/ ELECTROLYTES

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 5.5%;102MG/100ML;522MG/100ML;431MG/100ML;224MG/100ML

Packaging :

Approval Date : 1982-01-01

Application Number : 17493

Regulatory Info : DISCN

Registration Country : USA

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13

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

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

Brand Name : TRAVASOL 8.5% W/ ELECTROLYTES

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 8.5%;102MG/100ML;522MG/100ML;594MG/100ML;154MG/100ML

Packaging :

Approval Date : 1982-01-01

Application Number : 17493

Regulatory Info : DISCN

Registration Country : USA

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14

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

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

Brand Name : TRAVASOL 3.5% W/ ELECTROLYTES

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 3.5%;51MG/100ML;131MG/100ML;218MG/100ML;35MG/100ML

Packaging :

Approval Date : 1982-01-01

Application Number : 17493

Regulatory Info : DISCN

Registration Country : USA

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15

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

SODIUM ACETATE

Brand Name : CLINIMIX E

Dosage Form : SOLUTION

Dosage Strength : 205MG/100ML

Packaging : 2000ML

Approval Date :

Application Number : 2142384

Regulatory Info : Ethical

Registration Country : Canada

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16

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

SODIUM ACETATE

Brand Name : CLINIMIX E

Dosage Form : SOLUTION

Dosage Strength : 205MG/100ML

Packaging : 1000ML

Approval Date :

Application Number : 2013967

Regulatory Info : Ethical

Registration Country : Canada

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17

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

SODIUM ACETATE

Brand Name : CLINIMIX E

Dosage Form : SOLUTION

Dosage Strength : 205MG/100ML

Packaging : 1000ML

Approval Date :

Application Number : 2014076

Regulatory Info : Ethical

Registration Country : Canada

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18

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

SODIUM ACETATE

Brand Name : NEO-SULFALYTE

Dosage Form : BOLUS

Dosage Strength : 229MG

Packaging : 50

Approval Date :

Application Number : 641618

Regulatory Info : Prescription

Registration Country : Canada

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19

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

SODIUM ACETATE

Brand Name : SULFAVITE

Dosage Form : POWDER FOR SOLUTION

Dosage Strength : 2.5G/400G

Packaging : 400G/10KG

Approval Date :

Application Number : 721069

Regulatory Info : Prescription

Registration Country : Canada

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20

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

SODIUM DIACETATE

Brand Name : ELECTROVITE

Dosage Form : POWDER

Dosage Strength : 0.66MG/G

Packaging : 300G,10/18KG

Approval Date :

Application Number : 580007

Regulatory Info : OTC

Registration Country : Canada

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21

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

SODIUM ACETATE

Brand Name : ELECTROVITE

Dosage Form : POWDER

Dosage Strength : 0.33MG/G

Packaging : 300G,10/18KG

Approval Date :

Application Number : 580007

Regulatory Info : OTC

Registration Country : Canada

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22

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

SODIUM ACETATE

Brand Name : SODIUM ACETATE INJECTION, USP

Dosage Form : SOLUTION

Dosage Strength : 328MG/ML

Packaging : 50ML/100 ML

Approval Date :

Application Number : 2139529

Regulatory Info : Ethical

Registration Country : Canada

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23

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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24

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE

Brand Name : NORMOSOL-R IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 30MG/100ML;37MG/100ML;222MG/100ML;526MG/100ML;502MG/100ML

Packaging :

Approval Date : 1982-01-01

Application Number : 17586

Regulatory Info : RX

Registration Country : USA

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25

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE

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

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 5GM/100ML;30MG/100ML;37MG/100ML;222MG/100ML;526MG/100ML;502MG/100ML

Packaging :

Approval Date : 1982-01-01

Application Number : 17609

Regulatory Info : RX

Registration Country : USA

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26

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE

Brand Name : PHYSIOSOL IN PLASTIC CONTAINER

Dosage Form : SOLUTION;IRRIGATION

Dosage Strength : 30MG/100ML;37MG/100ML;222MG/100ML;526MG/100ML;502MG/100ML

Packaging :

Approval Date : 1982-07-08

Application Number : 17637

Regulatory Info : RX

Registration Country : USA

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27

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

SODIUM ACETATE

Brand Name : NORMOSOL-R

Dosage Form : SOLUTION

Dosage Strength : 0.222G/100ML

Packaging : 500ML/1000ML

Approval Date :

Application Number : 39500

Regulatory Info : Ethical

Registration Country : Canada

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28

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

SODIUM ACETATE

Brand Name : TPN ELECTROLYTES

Dosage Form : SOLUTION

Dosage Strength : 121MG/ML

Packaging : 20ML

Approval Date :

Application Number : 590215

Regulatory Info : Ethical

Registration Country : Canada

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29

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

SODIUM ACETATE

Brand Name : V-LYTES (WATER SOLUBLE ELECTROLYTE POWDER)

Dosage Form : POWDER FOR SOLUTION

Dosage Strength : 13.125G/80G

Packaging : 80GM/4KG

Approval Date :

Application Number : 2047519

Regulatory Info : OTC

Registration Country : Canada

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30

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

SODIUM ACETATE

Brand Name : V-LYTES HE (WATER SOLUBLE NUTRIENT, ELECTROLYTE POWDER FOR ORAL USE IN CALVES)

Dosage Form : POWDER FOR SOLUTION

Dosage Strength : 13.125G/184G

Packaging : 10X18.4G/3.7KG

Approval Date :

Application Number : 1957341

Regulatory Info : OTC

Registration Country : Canada

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