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01 4CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE

02 3NAFCILLIN SODIUM

03 4SOYBEAN OIL

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PharmaCompass

01

Brand Name : INPERSOL-LC/LM W/ DE...

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : INPERSOL-LC/LM W/ DE...

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Fresenius Medical Care

Dosage Form : SOLUTION; INTRAPERITONEAL

Proprietary Name : INPERSOL-LC/LM W/ DEXTRO...

Dosage Strength : 18.4MG/100ML;1.5GM/100ML...

Approval Date : 1994-06-13

Application Number : 20374

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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02

Brand Name : INPERSOL-LC/LM W/ DE...

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Brand Name : INPERSOL-LC/LM W/ DE...

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Fresenius Medical Care

Dosage Form : SOLUTION; INTRAPERITONEAL

Proprietary Name : INPERSOL-LC/LM W/ DEXTRO...

Dosage Strength : 18.4MG/100ML;2.5GM/100ML...

Approval Date : 1994-06-13

Application Number : 20374

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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03

Brand Name : INPERSOL-LC/LM W/ DE...

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Brand Name : INPERSOL-LC/LM W/ DE...

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Fresenius Medical Care

Dosage Form : SOLUTION; INTRAPERITONEAL

Proprietary Name : INPERSOL-LC/LM W/ DEXTRO...

Dosage Strength : 18.4MG/100ML;3.5GM/100ML...

Approval Date : 1994-06-13

Application Number : 20374

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

04

Brand Name : INPERSOL-LC/LM W/ DE...

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Brand Name : INPERSOL-LC/LM W/ DE...

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Fresenius Medical Care

Dosage Form : SOLUTION; INTRAPERITONEAL

Proprietary Name : INPERSOL-LC/LM W/ DEXTRO...

Dosage Strength : 18.4MG/100ML;4.25GM/100M...

Approval Date : 1994-06-13

Application Number : 20374

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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05

Brand Name : NAFCILLIN SODIUM

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Brand Name : NAFCILLIN SODIUM

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Fresenius Medical Care

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : NAFCILLIN SODIUM

Dosage Strength : EQ 1GM BASE/VIAL

Approval Date : 2019-12-10

Application Number : 206682

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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06

Brand Name : NAFCILLIN SODIUM

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Brand Name : NAFCILLIN SODIUM

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Fresenius Medical Care

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : NAFCILLIN SODIUM

Dosage Strength : EQ 2GM BASE/VIAL

Approval Date : 2019-12-10

Application Number : 206682

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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07

Brand Name : NAFCILLIN SODIUM

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Brand Name : NAFCILLIN SODIUM

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Fresenius Medical Care

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : NAFCILLIN SODIUM

Dosage Strength : EQ 10GM BASE/VIAL

Approval Date : 2020-06-02

Application Number : 206761

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

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08

Brand Name : INTRALIPID 10%

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : INTRALIPID 10%

Pharma, Lab & Chemical Expo
Not Confirmed
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Fresenius Medical Care

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : INTRALIPID 10%

Dosage Strength : 10%

Approval Date : 1982-01-01

Application Number : 17643

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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09

Brand Name : INTRALIPID 30%

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Brand Name : INTRALIPID 30%

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Fresenius Medical Care

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : INTRALIPID 30%

Dosage Strength : 30%

Approval Date : 1993-12-30

Application Number : 19942

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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10

Brand Name : INTRALIPID 20%

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Brand Name : INTRALIPID 20%

Pharma, Lab & Chemical Expo
Not Confirmed
arrow

Fresenius Medical Care

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : INTRALIPID 20%

Dosage Strength : 20%

Approval Date : 1996-08-07

Application Number : 20248

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AP

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