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01 2ACS DOBFAR SPA

02 3Advanz Pharma

03 2Apotex Inc

04 5Aurogen South Africa (Pty) Ltd

05 2B. Braun Medical

06 2Baxter Healthcare Corporation

07 2Belco Pharma

08 3Chartwell Pharmaceuticals llc

09 1Doctor's Life Sciences

10 4Fresenius SE & Co. KGaA

11 3Hikma Pharmaceuticals

12 8Hospira, Inc.

13 2Ldp Torlan Laboratories Sa

14 2MIP Pharma

15 3Qilu Antibiotics Pharmaceutical Co., Ltd.

16 2Qilu Pharmaceutical

17 2Reig Jofre

18 2Sagent Pharmaceuticals

19 1Samson Medical Technologies

20 2Sandoz B2B

21 1UpChen Therapeutics Limited

22 2XYZ Pharma

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PharmaCompass

01

VMX
Not Confirmed
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VMX
Not Confirmed

CEFEPIME HYDROCHLORIDE

Brand Name : CEFEPIME HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1GM BASE/VIAL

Packaging :

Approval Date : 2008-03-20

Application Number : 65441

Regulatory Info : RX

Registration Country : USA

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02

VMX
Not Confirmed
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VMX
Not Confirmed

CEFEPIME HYDROCHLORIDE

Brand Name : CEFEPIME HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2GM BASE/VIAL

Packaging :

Approval Date : 2008-03-20

Application Number : 65441

Regulatory Info : RX

Registration Country : USA

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03

VMX
Not Confirmed
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VMX
Not Confirmed

CEFEPIME HYDROCHLORIDE

Brand Name : CEFEPIME AND DEXTROSE IN DUPLEX CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1GM BASE/VIAL

Packaging :

Approval Date : 2010-05-06

Application Number : 50821

Regulatory Info : RX

Registration Country : USA

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04

VMX
Not Confirmed
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VMX
Not Confirmed

CEFEPIME HYDROCHLORIDE

Brand Name : CEFEPIME AND DEXTROSE IN DUPLEX CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2GM BASE/VIAL

Packaging :

Approval Date : 2010-05-06

Application Number : 50821

Regulatory Info : RX

Registration Country : USA

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05

VMX
Not Confirmed
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VMX
Not Confirmed

CEFEPIME HYDROCHLORIDE

Brand Name : CEFEPIME IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

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

Packaging :

Approval Date : 2008-08-05

Application Number : 50817

Regulatory Info : RX

Registration Country : USA

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06

VMX
Not Confirmed
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VMX
Not Confirmed

CEFEPIME HYDROCHLORIDE

Brand Name : CEFEPIME IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

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

Packaging :

Approval Date : 2008-08-05

Application Number : 50817

Regulatory Info : RX

Registration Country : USA

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07

VMX
Not Confirmed
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VMX
Not Confirmed

CEFEPIME HYDROCHLORIDE

Brand Name : CEFEPIME HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 500MG BASE/VIAL

Packaging :

Approval Date : 2010-12-21

Application Number : 90291

Regulatory Info : DISCN

Registration Country : USA

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08

VMX
Not Confirmed
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VMX
Not Confirmed

CEFEPIME HYDROCHLORIDE

Brand Name : CEFEPIME HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1GM BASE/VIAL

Packaging :

Approval Date : 2010-12-21

Application Number : 90291

Regulatory Info : DISCN

Registration Country : USA

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09

VMX
Not Confirmed
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VMX
Not Confirmed

CEFEPIME HYDROCHLORIDE

Brand Name : CEFEPIME HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2GM BASE/VIAL

Packaging :

Approval Date : 2010-12-21

Application Number : 90291

Regulatory Info : DISCN

Registration Country : USA

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10

VMX
Not Confirmed
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VMX
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**

Packaging :

Approval Date : 1996-01-18

Application Number : 50679

Regulatory Info : DISCN

Registration Country : USA

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11

VMX
Not Confirmed
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VMX
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**

Packaging :

Approval Date : 1996-01-18

Application Number : 50679

Regulatory Info : DISCN

Registration Country : USA

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12

VMX
Not Confirmed
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VMX
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**

Packaging :

Approval Date : 1996-01-18

Application Number : 50679

Regulatory Info : DISCN

Registration Country : USA

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13

VMX
Not Confirmed
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VMX
Not Confirmed

CEFEPIME HYDROCHLORIDE

Brand Name : CEFEPIME HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 500MG BASE/VIAL

Packaging :

Approval Date : 2007-06-18

Application Number : 65369

Regulatory Info : DISCN

Registration Country : USA

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14

VMX
Not Confirmed
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VMX
Not Confirmed

CEFEPIME HYDROCHLORIDE

Brand Name : CEFEPIME HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1GM BASE/VIAL

Packaging :

Approval Date : 2007-06-18

Application Number : 65369

Regulatory Info : DISCN

Registration Country : USA

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15

VMX
Not Confirmed
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VMX
Not Confirmed

CEFEPIME HYDROCHLORIDE

Brand Name : CEFEPIME HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2GM BASE/VIAL

Packaging :

Approval Date : 2007-06-18

Application Number : 65369

Regulatory Info : DISCN

Registration Country : USA

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16

VMX
Not Confirmed
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VMX
Not Confirmed

CEFEPIME HYDROCHLORIDE

Brand Name : CEFEPIME HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1GM BASE/VIAL

Packaging :

Approval Date : 2012-07-30

Application Number : 202268

Regulatory Info : DISCN

Registration Country : USA

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17

VMX
Not Confirmed
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VMX
Not Confirmed

CEFEPIME HYDROCHLORIDE

Brand Name : CEFEPIME HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2GM BASE/VIAL

Packaging :

Approval Date : 2012-07-30

Application Number : 202268

Regulatory Info : DISCN

Registration Country : USA

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18

VMX
Not Confirmed
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VMX
Not Confirmed

CEFEPIME HYDROCHLORIDE

Brand Name : CEFEPIME HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 500MG BASE/VIAL

Packaging :

Approval Date : 2016-02-01

Application Number : 203704

Regulatory Info : RX

Registration Country : USA

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19

VMX
Not Confirmed
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VMX
Not Confirmed

CEFEPIME HYDROCHLORIDE

Brand Name : CEFEPIME HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1GM BASE/VIAL

Packaging :

Approval Date : 2017-01-04

Application Number : 91048

Regulatory Info : RX

Registration Country : USA

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20

VMX
Not Confirmed
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VMX
Not Confirmed

CEFEPIME HYDROCHLORIDE

Brand Name : CEFEPIME HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2GM BASE/VIAL

Packaging :

Approval Date : 2017-01-04

Application Number : 91048

Regulatory Info : RX

Registration Country : USA

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