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01 1Abbott Laboratories

02 97Adcock Ingram

03 1Al-Razi Pharma

04 20B. Braun Medical

05 59Baxter Healthcare Corporation

06 2DMVET INC

07 2Demo S.A.

08 20Fresenius Kabi AB Brunna

09 1Fresenius Kabi AG

10 3Fresenius Kabi USA

11 4Fresenius Medical Care

12 3Fresenius Medical Care de Mexico

13 10Fresenius SE & Co. KGaA

14 3Hospira, Inc.

15 14ICU Medical

16 4Igenius Life Sciences

17 2LeBasi Pharmaceuticals CC

18 2MILES

19 1MONICO SpA

20 6NXSTAGE MEDICAL INC

21 1PROCTER AND GAMBLE

22 18SALF SpA

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PharmaCompass

01

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

Sodium lactate

Brand Name : Sabax Pethidine 50 mg

Dosage Form : INJ

Dosage Strength : 5g/1000ml

Packaging : 10X1mg/ml

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Africa

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02

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

Sodium lactate

Brand Name : Pectrolyte

Dosage Form : SUS

Dosage Strength : 20ml

Packaging : 150X1ml/100ml

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Africa

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03

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE

Brand Name : DEXTROSE 5% IN LACTATED RINGERS IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 20MG/100ML;5GM/100ML;30MG/100ML;600MG/100ML;310MG/100ML

Packaging :

Approval Date : 1982-01-01

Application Number : 17510

Regulatory Info : DISCN

Registration Country : USA

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04

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

Sodium Lactate

Brand Name : Ringer Lactate Infusion B.Braun

Dosage Form : INF

Dosage Strength : 3.2g/1000ml

Packaging : 200X1g/1000ml

Approval Date :

Application Number :

Regulatory Info : Originator

Registration Country : South Africa

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05

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

Sodium Lactate

Brand Name : Ringer Lactate Infusion B.Braun

Dosage Form : INF

Dosage Strength : 3.2g/1000ml

Packaging : 1000X1g/1000ml

Approval Date :

Application Number :

Regulatory Info : Originator

Registration Country : South Africa

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06

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

Sodium Lactate

Brand Name : Ringer's Lactate B.Braun

Dosage Form : INF

Dosage Strength : 3.12g/1000ml

Packaging : 1000X1g/1000ml

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Africa

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07

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

Sodium Lactate

Brand Name : Ringer's Lactate B.Braun

Dosage Form : INF

Dosage Strength : 3.12g/1000ml

Packaging : 1000X10g/1000ml

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Africa

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08

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE

Brand Name : LACTATED RINGERS AND DEXTROSE 5% IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 20MG/100ML;5GM/100ML;30MG/100ML;600MG/100ML;310MG/100ML

Packaging :

Approval Date : 1982-01-01

Application Number : 16679

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; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE

Brand Name : LACTATED RINGERS IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 20MG/100ML;30MG/100ML;600MG/100ML;310MG/100ML

Packaging :

Approval Date : 1982-01-01

Application Number : 16682

Regulatory Info : RX

Registration Country : USA

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10

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

SODIUM LACTATE

Brand Name : SODIUM LACTATE 0.167 MOLAR IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 1.87GM/100ML

Packaging :

Approval Date : 1982-01-01

Application Number : 16692

Regulatory Info : DISCN

Registration Country : USA

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11

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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12

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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13

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, MONOBASIC; SODIUM CHLORIDE; SODIUM LACTATE

Brand Name : DEXTROSE 5% AND ELECTROLYTE NO. 48 IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 5GM/100ML;31MG/100ML;141MG/100ML;20MG/100ML;12MG/100ML;260MG/100ML

Packaging :

Approval Date : 1982-01-01

Application Number : 17484

Regulatory Info : RX

Registration Country : USA

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14

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE

Brand Name : DIANEAL 137 W/ DEXTROSE 1.5% IN PLASTIC CONTAINER

Dosage Form : SOLUTION;INTRAPERITONEAL

Dosage Strength : 25.7MG/100ML;1.5GM/100ML;15.2MG/100ML;567MG/100ML;392MG/100ML

Packaging :

Approval Date : 1982-01-01

Application Number : 17512

Regulatory Info : DISCN

Registration Country : USA

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15

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE

Brand Name : DIANEAL 137 W/ DEXTROSE 4.25% IN PLASTIC CONTAINER

Dosage Form : SOLUTION;INTRAPERITONEAL

Dosage Strength : 25.7MG/100ML;4.25GM/100ML;15.2MG/100ML;567MG/100ML;392MG/100ML

Packaging :

Approval Date : 1982-01-01

Application Number : 17512

Regulatory Info : DISCN

Registration Country : USA

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16

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE

Brand Name : DIANEAL 137 W/ DEXTROSE 2.5% IN PLASTIC CONTAINER

Dosage Form : SOLUTION;INTRAPERITONEAL

Dosage Strength : 25.7MG/100ML;2.5GM/100ML;15.2MG/100ML;567MG/100ML;392MG/100ML

Packaging :

Approval Date : 1982-01-01

Application Number : 17512

Regulatory Info : DISCN

Registration Country : USA

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17

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE

Brand Name : DIANEAL PD-2 W/ DEXTROSE 1.5% IN PLASTIC CONTAINER

Dosage Form : SOLUTION;INTRAPERITONEAL

Dosage Strength : 25.7MG/100ML;1.5GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

Packaging :

Approval Date : 1982-01-01

Application Number : 17512

Regulatory Info : RX

Registration Country : USA

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18

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE

Brand Name : DIANEAL PD-2 W/ DEXTROSE 2.5% IN PLASTIC CONTAINER

Dosage Form : SOLUTION;INTRAPERITONEAL

Dosage Strength : 25.7MG/100ML;2.5GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

Packaging :

Approval Date : 1982-01-01

Application Number : 17512

Regulatory Info : RX

Registration Country : USA

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19

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE

Brand Name : DIANEAL PD-2 W/ DEXTROSE 4.25% IN PLASTIC CONTAINER

Dosage Form : SOLUTION;INTRAPERITONEAL

Dosage Strength : 25.7MG/100ML;4.25GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML

Packaging :

Approval Date : 1982-01-01

Application Number : 17512

Regulatory Info : RX

Registration Country : USA

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20

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE

Brand Name : DIANEAL PD-1 W/ DEXTROSE 1.5% IN PLASTIC CONTAINER

Dosage Form : SOLUTION;INTRAPERITONEAL

Dosage Strength : 25.7MG/100ML;1.5GM/100ML;15.2MG/100ML;567MG/100ML;392MG/100ML

Packaging :

Approval Date : 1984-07-09

Application Number : 17512

Regulatory Info : DISCN

Registration Country : USA

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21

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE

Brand Name : DIANEAL PD-1 W/ DEXTROSE 2.5% IN PLASTIC CONTAINER

Dosage Form : SOLUTION;INTRAPERITONEAL

Dosage Strength : 25.7MG/100ML;2.5GM/100ML;15.2MG/100ML;567MG/100ML;392MG/100ML

Packaging :

Approval Date : 1984-07-09

Application Number : 17512

Regulatory Info : DISCN

Registration Country : USA

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22

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

Sodium Lactate

Brand Name : Modified Ringer-Lactate Solution with Dextrose 5% Fresenius

Dosage Form : INF

Dosage Strength : 6g

Packaging : 1000X1g

Approval Date :

Application Number :

Regulatory Info : Originator

Registration Country : South Africa

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23

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

Sodium Lactate

Brand Name : Modified Ringer-Lactate Solution with Dextrose 5% Fresenius

Dosage Form : INF

Dosage Strength : 6g

Packaging : 1000X12g

Approval Date :

Application Number :

Regulatory Info : Originator

Registration Country : South Africa

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24

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

Sodium lactate

Brand Name : ITN 3004 A

Dosage Form : INF

Dosage Strength : 1g

Packaging : 1X1ZZZ

Approval Date :

Application Number :

Regulatory Info : Originator

Registration Country : South Africa

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25

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

Sodium lactate

Brand Name : ITN 3004 A

Dosage Form : INF

Dosage Strength : 1g

Packaging : 1X1ZZZ

Approval Date :

Application Number :

Regulatory Info : Originator

Registration Country : South Africa

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26

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

Sodium lactate

Brand Name : Capd /Dpca 2

Dosage Form : SOL

Dosage Strength : 50mg/5 ml

Packaging : 2000X1g/1000ml

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Africa

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27

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

Sodium lactate

Brand Name : Capd/ Dpca 3

Dosage Form : SOL

Dosage Strength : 50mg/5 ml

Packaging : 2000X1g/1000ml

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Africa

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28

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

Sodium lactate

Brand Name : Capd/ Dpca 4

Dosage Form : SOL

Dosage Strength : 50mg/5 ml

Packaging : 2000X1g/1000ml

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Africa

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29

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

Sodium lactate

Brand Name : Capd/ Dpca 17

Dosage Form : SOL

Dosage Strength : 50mg/5 ml

Packaging : 2000X1g/1000ml

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Africa

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30

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

Sodium lactate

Brand Name : Capd/ Dpca 18

Dosage Form : SOL

Dosage Strength : 50mg/5 ml

Packaging : 2000X1g/1000ml

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Africa

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