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01 2ACS DOBFAR SPA
02 2Advanz Pharma
03 2Apotex Inc
04 4Aurogen 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 3Qilu Antibiotics Pharmaceutical Co., Ltd.
15 2Qilu Pharmaceutical
16 2Reig Jofre
17 2Sagent Pharmaceuticals
18 1Samson Medical Technologies
19 2Sandoz B2B
20 1UpChen Therapeutics Limited
21 2XYZ Pharma
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01 10INJ
02 26INJECTABLE;INJECTION
03 3Injection
04 3POWDER FOR SOLUTION
05 1POWDER;INTRAVENOUS
06 1Powder For Concentrate For Infusion Solution
07 1Powder For Concentrate For Solution For Infusion
08 6Powder For Injection And Infusion Solution
09 1Powder for Injection
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01 1Approved
02 7Authorized
03 13DISCN
04 10Generic
05 3Prescription
06 14RX
07 4Blank
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01 2APO-CEFEPIME
02 2Auro Cefepime Injection 1000 mg
03 2Auro Cefepime Injection 2000 mg
04 2CEFEPIME 1g FRESENIUS
05 2CEFEPIME 2g FRESENIUS
06 2CEFEPIME AND DEXTROSE IN DUPLEX CONTAINER
07 1CEFEPIME FOR INJECTION USP
08 19CEFEPIME HYDROCHLORIDE
09 1CEFEPIME HYDROCHLORIDE IN PLASTIC CONTAINER
10 2CEFEPIME IN PLASTIC CONTAINER
11 1CRITIPEME 1000
12 1CRITIPEME 2000
13 2Cefepima Ldp- Laboratorios Torlan
14 2Cefepima Qilu
15 2Cefepima Sala
16 1ESPIM-0.5g INJECTION
17 1ESPIM-1g INJECTION
18 2Exblifep
19 3MAXIPIME
20 1Pime-SB
21 1Blank
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01 3Canada
02 3India
03 10South Africa
04 7Spain
05 1Sweden
06 1Taiwan
07 27USA
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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