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01 2ACS DOBFAR

02 2ASTRAL

03 2B BRAUN

04 2BAXTER HLTHCARE

05 3CHARTWELL RX

06 2HIKMA

07 8HOSPIRA INC

08 3QILU

09 2SAGENT PHARMS INC

10 1SAMSON MEDCL

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PharmaCompass

01

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

CEFEPIME HYDROCHLORIDE

Brand Name : CEFEPIME AND DEXTROSE IN DUPLEX CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1GM BASE/VIAL

Approval Date : 2010-05-06

Application Number : 50821

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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02

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

CEFEPIME HYDROCHLORIDE

Brand Name : CEFEPIME AND DEXTROSE IN DUPLEX CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2GM BASE/VIAL

Approval Date : 2010-05-06

Application Number : 50821

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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03

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

CEFEPIME HYDROCHLORIDE

Brand Name : CEFEPIME IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1GM BASE/50ML (EQ 20MG BASE/ML)

Approval Date : 2008-08-05

Application Number : 50817

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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04

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

CEFEPIME HYDROCHLORIDE

Brand Name : CEFEPIME IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2GM BASE/100ML (EQ 20MG BASE/ML)

Approval Date : 2008-08-05

Application Number : 50817

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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05

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

CEFEPIME HYDROCHLORIDE

Brand Name : MAXIPIME

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1996-01-18

Application Number : 50679

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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06

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

CEFEPIME HYDROCHLORIDE

Brand Name : MAXIPIME

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1996-01-18

Application Number : 50679

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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07

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

CEFEPIME HYDROCHLORIDE

Brand Name : MAXIPIME

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1996-01-18

Application Number : 50679

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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08

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

CEFEPIME HYDROCHLORIDE

Brand Name : CEFEPIME HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 500MG BASE/VIAL

Approval Date : 2007-06-18

Application Number : 65369

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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09

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

CEFEPIME HYDROCHLORIDE

Brand Name : CEFEPIME HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1GM BASE/VIAL

Approval Date : 2007-06-18

Application Number : 65369

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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10

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

CEFEPIME HYDROCHLORIDE

Brand Name : CEFEPIME HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2GM BASE/VIAL

Approval Date : 2007-06-18

Application Number : 65369

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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