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 4Fresenius SE & Co. KGaA
09 3Hikma Pharmaceuticals
10 8Hospira, Inc.
11 2MIP Pharma
12 3Qilu Pharmaceutical
13 2Sagent Pharmaceuticals
14 1Samson Medical Technologies
15 2Sandoz B2B
16 1UpChen Therapeutics Limited
17 2XYZ Pharma
01 8INJ
02 26INJECTABLE;INJECTION
03 2Injection
04 2POWDER FOR INJECTION / INFUSION
05 3POWDER FOR SOLUTION
06 1POWDER;INTRAVENOUS
07 1Powder for Injection
01 13DISCN
02 8Generic
03 3Prescription
04 14RX
05 5Blank
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 2cefepime MIP
17 1Blank
01 3Canada
02 2India
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 : RX
Registration Country : USA
Brand Name : CEFEPIME HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1GM BASE/VIAL
Packaging :
Approval Date : 2024-05-22
Application Number : 214402
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 : 2024-05-22
Application Number : 214402
Regulatory Info : RX
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 :
Registration Country : Sweden
cefepime dihydrochloride monohydrate
Brand Name : cefepime MIP
Dosage Form : POWDER FOR INJECTION / INFUSION
Dosage Strength : 2 G
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Sweden
cefepime dihydrochloride monohydrate
Brand Name : cefepime MIP
Dosage Form : POWDER FOR INJECTION / INFUSION
Dosage Strength : 1 G
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
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 : 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 2GM 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
Regulatory Info : RX
Registration Country : USA
Brand Name : CEFEPIME HYDROCHLORIDE IN PLASTIC CONTAINER
Dosage Form : POWDER;INTRAVENOUS
Dosage Strength : EQ 100GM BASE
Packaging :
Approval Date : 2018-08-21
Application Number : 209408
Regulatory Info : RX
Registration Country : USA
Regulatory Info :
Registration Country : Taiwan
Brand Name :
Dosage Form : Powder for Injection
Dosage Strength : 1000MG
Packaging : Box x 10 Vials
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Taiwan
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CEFEPIME HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1GM BASE/VIAL
Packaging :
Approval Date : 2020-07-21
Application Number : 212721
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 : 2020-07-21
Application Number : 212721
Regulatory Info : DISCN
Registration Country : USA
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