01 3ACS DOBFAR SPA
02 3Antibiotice SA
03 5Aurobindo Pharma Limited
04 2Bio Labs
05 1Entasis Therapeutics
06 3HQ SPECLT PHARMA
07 2Hainan Haiyao
08 3Hikma Pharmaceuticals
09 5Hospira, Inc.
10 3Istituto Biochimico Italiano Giovanni Lorenzini SpA
11 2MEDIMETRIKS PHARMS
12 6Pfizer Inc
13 3STERISCIENCE SPECLTS
14 5Sandoz B2B
15 3XYZ Pharma
16 8Xiangbei Welman Pharmaceuticals
17 2Yangtze River Pharmaceutical Group
01 43INJECTABLE;INJECTION
02 2INJECTION
03 12Injection
04 1POWDER;INTRAVENOUS
05 1powder for injection/Infusion
01 15DISCN
02 2Generic
03 29RX
04 13Blank
01 1 AMPIPLUS®
02 37AMPICILLIN AND SULBACTAM
03 2Sulperazone
04 6UNASYN
05 1XACDURO (COPACKAGED)
06 12Blank
01 12China
02 2Pakistan
03 1Romania
04 44USA
Regulatory Info : RX
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Brand Name : AMPICILLIN AND SULBACTAM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 10GM BASE/VIAL;EQ 5GM BASE/VIAL
Packaging :
Approval Date : 2009-12-23
Application Number : 65403
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Brand Name : AMPICILLIN AND SULBACTAM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1GM BASE/VIAL;EQ 500MG BASE/VIAL
Packaging :
Approval Date : 2009-12-22
Application Number : 65406
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Brand Name : AMPICILLIN AND SULBACTAM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 2GM BASE/VIAL;EQ 1GM BASE/VIAL
Packaging :
Approval Date : 2009-12-22
Application Number : 65406
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Brand Name : AMPICILLIN AND SULBACTAM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 10GM BASE/VIAL;EQ 5GM BASE/VIAL
Packaging :
Approval Date : 2010-09-20
Application Number : 90339
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Brand Name : AMPICILLIN AND SULBACTAM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1GM BASE/VIAL;EQ 500MG BASE/VIAL
Packaging :
Approval Date : 2010-09-20
Application Number : 90340
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Brand Name : AMPICILLIN AND SULBACTAM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 2GM BASE/VIAL;EQ 1GM BASE/VIAL
Packaging :
Approval Date : 2010-09-20
Application Number : 90340
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Brand Name : AMPICILLIN AND SULBACTAM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1GM BASE/VIAL;EQ 500MG BASE/VIAL
Packaging :
Approval Date : 2010-09-20
Application Number : 90349
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Brand Name : AMPICILLIN AND SULBACTAM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 2GM BASE/VIAL;EQ 1GM BASE/VIAL
Packaging :
Approval Date : 2010-09-20
Application Number : 90349
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Brand Name : AMPICILLIN AND SULBACTAM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1GM BASE/VIAL;EQ 500MG BASE/VIAL
Packaging :
Approval Date : 2002-03-19
Application Number : 65074
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Brand Name : AMPICILLIN AND SULBACTAM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 2GM BASE/VIAL;EQ 1GM BASE/VIAL
Packaging :
Approval Date : 2002-03-19
Application Number : 65074
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Brand Name : AMPICILLIN AND SULBACTAM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 10GM BASE/VIAL;EQ 5GM BASE/VIAL
Packaging :
Approval Date : 2002-03-19
Application Number : 65076
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Brand Name : AMPICILLIN AND SULBACTAM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1GM BASE/VIAL;EQ 500MG BASE/VIAL
Packaging :
Approval Date : 2005-11-30
Application Number : 65176
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Brand Name : AMPICILLIN AND SULBACTAM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 2GM BASE/VIAL;EQ 1GM BASE/VIAL
Packaging :
Approval Date : 2005-11-30
Application Number : 65176
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Brand Name : AMPICILLIN AND SULBACTAM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 10GM BASE/VIAL;EQ 5GM BASE/VIAL
Packaging :
Approval Date : 2005-11-25
Application Number : 65188
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Brand Name : AMPICILLIN AND SULBACTAM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1GM BASE/VIAL;EQ 500MG BASE/VIAL
Packaging :
Approval Date : 2005-11-29
Application Number : 65222
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Brand Name : AMPICILLIN AND SULBACTAM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 2GM BASE/VIAL;EQ 1GM BASE/VIAL
Packaging :
Approval Date : 2005-11-29
Application Number : 65222
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Brand Name : AMPICILLIN AND SULBACTAM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 10GM BASE/VIAL;EQ 5GM BASE/VIAL
Packaging :
Approval Date : 2006-11-27
Application Number : 65314
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Brand Name : AMPICILLIN AND SULBACTAM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1GM BASE/VIAL;EQ 500MG BASE/VIAL
Packaging :
Approval Date : 2007-06-29
Application Number : 65316
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Brand Name : AMPICILLIN AND SULBACTAM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 2GM BASE/VIAL;EQ 1GM BASE/VIAL
Packaging :
Approval Date : 2007-06-29
Application Number : 65316
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Brand Name : UNASYN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 2GM BASE/VIAL;EQ 1GM BASE/VIAL
Packaging :
Approval Date : 1986-12-31
Application Number : 50608
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Brand Name : UNASYN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1GM BASE/VIAL;EQ 500MG BASE/VIAL
Packaging :
Approval Date : 1986-12-31
Application Number : 50608
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Brand Name : UNASYN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG BASE/VIAL;EQ 250MG BASE/VIAL
Packaging :
Approval Date : 1986-12-31
Application Number : 50608
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Brand Name : UNASYN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 10GM BASE/VIAL;EQ 5GM BASE/VIAL
Packaging :
Approval Date : 1993-12-10
Application Number : 50608
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Brand Name : UNASYN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1GM BASE/VIAL;EQ 500MG BASE/VIAL
Packaging :
Approval Date : 1988-11-23
Application Number : 62901
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Brand Name : UNASYN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 2GM BASE/VIAL;EQ 1GM BASE/VIAL
Packaging :
Approval Date : 1992-02-27
Application Number : 62901
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Brand Name : AMPICILLIN AND SULBACTAM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 10GM BASE/VIAL;EQ 5GM BASE/VIAL
Packaging :
Approval Date : 2006-07-25
Application Number : 65240
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Brand Name : AMPICILLIN AND SULBACTAM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1GM BASE/VIAL;EQ 500MG BASE/VIAL
Packaging :
Approval Date : 2006-07-25
Application Number : 65241
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Brand Name : AMPICILLIN AND SULBACTAM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 2GM BASE/VIAL;EQ 1GM BASE/VIAL
Packaging :
Approval Date : 2006-07-25
Application Number : 65241
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Brand Name : AMPICILLIN AND SULBACTAM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1GM BASE/VIAL;EQ 500MG BASE/VIAL
Packaging :
Approval Date : 2006-07-25
Application Number : 65310
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMPICILLIN SODIUM; SULBACTAM SODIUM
Brand Name : AMPICILLIN AND SULBACTAM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 2GM BASE/VIAL;EQ 1GM BASE/VIAL
Packaging :
Approval Date : 2006-07-25
Application Number : 65310
Regulatory Info : RX
Registration Country : USA
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