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
01 26INJECTABLE;INJECTION
02 1POWDER;INTRAVENOUS
01 13DISCN
02 14RX
01 2CEFEPIME AND DEXTROSE IN DUPLEX CONTAINER
02 19CEFEPIME HYDROCHLORIDE
03 1CEFEPIME HYDROCHLORIDE IN PLASTIC CONTAINER
04 2CEFEPIME IN PLASTIC CONTAINER
05 3MAXIPIME
01 20No
02 7Yes
RLD : Yes
TE Code :
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 :
RLD : Yes
TE Code :
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 :
RLD : Yes
TE Code :
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 :
RLD : Yes
TE Code :
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 :
RLD : Yes
TE Code :
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Dosage Strength : EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
RLD : Yes
TE Code :
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Dosage Strength : EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
RLD : Yes
TE Code :
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Dosage Strength : EQ 2GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
RLD : No
TE Code :
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 :
RLD : No
TE Code :
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 :
RLD : No
TE Code :
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 :
LOOKING FOR A SUPPLIER?