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01 2ACS DOBFAR SPA
02 2Apotex Inc
03 2Aurogen South Africa (Pty) Ltd
04 2B. Braun Medical
05 2Baxter Healthcare Corporation
06 2Belco Pharma
07 3Chartwell Pharmaceuticals llc
08 1Doctor's Life Sciences
09 4Fresenius SE & Co. KGaA
10 3Hikma Pharmaceuticals
11 8Hospira, Inc.
12 2MIP Pharma
13 3Qilu Antibiotics Pharmaceutical Co., Ltd.
14 2Sagent Pharmaceuticals
15 1Samson Medical Technologies
16 2Sandoz B2B
17 1UpChen Therapeutics Limited
18 2XYZ Pharma
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01 8INJ
02 26INJECTABLE;INJECTION
03 3Injection
04 2POWDER FOR INJECTION / INFUSION
05 3POWDER FOR SOLUTION
06 1POWDER;INTRAVENOUS
07 1Powder for Injection
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01 13DISCN
02 8Generic
03 3Prescription
04 14RX
05 6Blank
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01 2APO-CEFEPIME
02 1Auro Cefepime Injection 1000 mg
03 1Auro 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 1ESPIM-0.5g INJECTION
14 1ESPIM-1g INJECTION
15 3MAXIPIME
16 1Pime-SB
17 2cefepime MIP
18 1Blank
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01 3Canada
02 3India
03 8South Africa
04 2Sweden
05 1Taiwan
06 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