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01 6MEDEFIL INC

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PharmaCompass

01

Brand Name : SODIUM CHLORIDE 0.9%

BePharma
Not Confirmed
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Brand Name : SODIUM CHLORIDE 0.9%

BePharma
Not Confirmed
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Medefil

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : SODIUM CHLORIDE 0.9%

Dosage Strength : 18MG/2ML (9MG/ML)

Approval Date : 2012-01-06

Application Number : 202832

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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02

Brand Name : SODIUM CHLORIDE 0.9%

BePharma
Not Confirmed
arrow

Brand Name : SODIUM CHLORIDE 0.9%

BePharma
Not Confirmed
arrow

Medefil

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : SODIUM CHLORIDE 0.9%

Dosage Strength : 45MG/5ML (9MG/ML)

Approval Date : 2012-01-06

Application Number : 202832

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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03

Brand Name : SODIUM CHLORIDE 0.9%

BePharma
Not Confirmed
arrow

Brand Name : SODIUM CHLORIDE 0.9%

BePharma
Not Confirmed
arrow

Medefil

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : SODIUM CHLORIDE 0.9%

Dosage Strength : 22.5MG/2.5ML (9MG/ML)

Approval Date : 2012-01-06

Application Number : 202832

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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04

Brand Name : SODIUM CHLORIDE 0.9%

BePharma
Not Confirmed
arrow

Brand Name : SODIUM CHLORIDE 0.9%

BePharma
Not Confirmed
arrow

Medefil

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : SODIUM CHLORIDE 0.9%

Dosage Strength : 9MG/ML (9MG/ML)

Approval Date : 2012-01-06

Application Number : 202832

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

05

Brand Name : SODIUM CHLORIDE 0.9%

BePharma
Not Confirmed
arrow

Brand Name : SODIUM CHLORIDE 0.9%

BePharma
Not Confirmed
arrow

Medefil

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : SODIUM CHLORIDE 0.9%

Dosage Strength : 90MG/10ML (9MG/ML)

Approval Date : 2012-01-06

Application Number : 202832

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

blank

06

Brand Name : SODIUM CHLORIDE 0.9%

BePharma
Not Confirmed
arrow

Brand Name : SODIUM CHLORIDE 0.9%

BePharma
Not Confirmed
arrow

Medefil

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : SODIUM CHLORIDE 0.9%

Dosage Strength : 27MG/3ML (9MG/ML)

Approval Date : 2012-01-06

Application Number : 202832

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank