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01 1ABBOTT

02 15B BRAUN

03 40BAXTER HLTHCARE

04 4FRESENIUS

05 3FRESENIUS KABI USA

06 20FRESENIUS MEDCL

07 3HOSPIRA

08 12ICU MEDICAL INC

09 2MILES

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PharmaCompass

01

BMWS24
Not Confirmed
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BMWS24
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

Approval Date : 1982-01-01

Application Number : 17510

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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02

BMWS24
Not Confirmed
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BMWS24
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

Approval Date : 1982-01-01

Application Number : 16679

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

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03

BMWS24
Not Confirmed
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BMWS24
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

Approval Date : 1982-01-01

Application Number : 16682

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AP

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04

BMWS24
Not Confirmed
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BMWS24
Not Confirmed

SODIUM LACTATE

Brand Name : SODIUM LACTATE 0.167 MOLAR IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 1.87GM/100ML

Approval Date : 1982-01-01

Application Number : 16692

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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05

BMWS24
Not Confirmed
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BMWS24
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**

Approval Date : 1982-01-01

Application Number : 17390

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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06

BMWS24
Not Confirmed
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BMWS24
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

Approval Date : 1982-01-01

Application Number : 17438

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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07

BMWS24
Not Confirmed
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BMWS24
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

Approval Date : 1982-01-01

Application Number : 17484

RX/OTC/DISCN : RX

RLD : No

TE Code :

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08

BMWS24
Not Confirmed
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BMWS24
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

Approval Date : 1982-01-01

Application Number : 17512

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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09

BMWS24
Not Confirmed
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BMWS24
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

Approval Date : 1982-01-01

Application Number : 17512

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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10

BMWS24
Not Confirmed
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BMWS24
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

Approval Date : 1982-01-01

Application Number : 17512

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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