Istituto Biochimico Italiano Giovanni Lorenzini SpA RX
FDA Approved Drugs

Istituto Biochimico Italiano Giovanni Lorenzini SpA RX

FDA Approved Drugs Database

FDA approved drug product records including application numbers, product numbers, drug names, active ingredients, dosage forms, strengths, approval dates and regulatory status.

RX
  • Total Records 21
  • Latest Approval Date Dec 20, 2013
  • Data Source FDA
  • First Approval Date May 12, 1987
All
27
View
Discontinued
6
View
RX
21
View
Company Overview

Company

Istituto Biochimico Italiano Giovanni Lorenzini SpA RX

Country

Italy

Website

Visit Website

Email

 info@ibi-lorenzini.com

Social Profiles

Company Snapshot

Istituto Biochimico Italiano Giovanni Lorenzini SpA RX

Istituto Biochimico Italiano Giovanni Lorenzini S.p.a. Via Fossignano 2, 04011 Aprilia(LT) , Italy

Italy

www.ibi-lorenzini.it/it  info@ibi-lorenzini.com View on Map
FDA Approved Drug Records ( 21 records )
2005
29 Nov
RX Application: 65222

Drug Name

AMPICILLIN AND SULBACTAM

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL;EQ 500MG BASE/VIAL

Approval Date

2005-11-29

65222 / 1

Active Ingredient

AMPICILLIN SODIUM; SULBACTAM SODIUM

Application Number

65222

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL;EQ 500MG BASE/VIAL

Approval Date

2005-11-29

Regulatory Status

RX

2005
29 Nov
RX Application: 65222

Drug Name

AMPICILLIN AND SULBACTAM

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL;EQ 1GM BASE/VIAL

Approval Date

2005-11-29

65222 / 2

Active Ingredient

AMPICILLIN SODIUM; SULBACTAM SODIUM

Application Number

65222

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL;EQ 1GM BASE/VIAL

Approval Date

2005-11-29

Regulatory Status

RX

2006
27 Nov
RX Application: 65314

Drug Name

AMPICILLIN AND SULBACTAM

Product Number

1

Dosage Form

-

Strength

EQ 10GM BASE/VIAL;EQ 5GM BASE/VIAL

Approval Date

2006-11-27

65314 / 1

Active Ingredient

AMPICILLIN SODIUM; SULBACTAM SODIUM

Application Number

65314

Product Number

1

Dosage Form

-

Strength

EQ 10GM BASE/VIAL;EQ 5GM BASE/VIAL

Approval Date

2006-11-27

Regulatory Status

RX

1987
12 May
RX Application: 62719

Drug Name

AMPICILLIN SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE/VIAL

Approval Date

1987-05-12

62719 / 1

Active Ingredient

AMPICILLIN SODIUM

Application Number

62719

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE/VIAL

Approval Date

1987-05-12

Regulatory Status

RX

1987
12 May
RX Application: 62719

Drug Name

AMPICILLIN SODIUM

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1987-05-12

62719 / 2

Active Ingredient

AMPICILLIN SODIUM

Application Number

62719

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1987-05-12

Regulatory Status

RX

1987
12 May
RX Application: 62719

Drug Name

AMPICILLIN SODIUM

Product Number

3

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1987-05-12

62719 / 3

Active Ingredient

AMPICILLIN SODIUM

Application Number

62719

Product Number

3

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1987-05-12

Regulatory Status

RX

1993
12 Jul
RX Application: 62797

Drug Name

AMPICILLIN SODIUM

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

1993-07-12

62797 / 2

Active Ingredient

AMPICILLIN SODIUM

Application Number

62797

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

1993-07-12

Regulatory Status

RX

2013
20 Dec
RX Application: 201404

Drug Name

AMPICILLIN SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 10GM BASE/VIAL

Approval Date

2013-12-20

201404 / 1

Active Ingredient

AMPICILLIN SODIUM

Application Number

201404

Product Number

1

Dosage Form

-

Strength

EQ 10GM BASE/VIAL

Approval Date

2013-12-20

Regulatory Status

RX

2011
30 Jun
RX Application: 90002

Drug Name

NAFCILLIN SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2011-06-30

90002 / 1

Active Ingredient

NAFCILLIN SODIUM

Application Number

90002

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2011-06-30

Regulatory Status

RX

2011
30 Jun
RX Application: 90002

Drug Name

NAFCILLIN SODIUM

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

2011-06-30

90002 / 2

Active Ingredient

NAFCILLIN SODIUM

Application Number

90002

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

2011-06-30

Regulatory Status

RX

2011
20 Apr
RX Application: 90005

Drug Name

NAFCILLIN SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 10GM BASE/VIAL

Approval Date

2011-04-20

90005 / 1

Active Ingredient

NAFCILLIN SODIUM

Application Number

90005

Product Number

1

Dosage Form

-

Strength

EQ 10GM BASE/VIAL

Approval Date

2011-04-20

Regulatory Status

RX

2009
18 Aug
RX Application: 65448

Drug Name

PENICILLIN G POTASSIUM

Product Number

1

Dosage Form

-

Strength

5,000,000 UNITS/VIAL

Approval Date

2009-08-18

65448 / 1

Active Ingredient

PENICILLIN G POTASSIUM

Application Number

65448

Product Number

1

Dosage Form

-

Strength

5,000,000 UNITS/VIAL

Approval Date

2009-08-18

Regulatory Status

RX

2009
18 Aug
RX Application: 65448

Drug Name

PENICILLIN G POTASSIUM

Product Number

2

Dosage Form

-

Strength

20,000,000 UNITS/VIAL

Approval Date

2009-08-18

65448 / 2

Active Ingredient

PENICILLIN G POTASSIUM

Application Number

65448

Product Number

2

Dosage Form

-

Strength

20,000,000 UNITS/VIAL

Approval Date

2009-08-18

Regulatory Status

RX

2003
14 Nov
RX Application: 65114

Drug Name

PIPERACILLIN

Product Number

1

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

2003-11-14

65114 / 1

Active Ingredient

PIPERACILLIN SODIUM

Application Number

65114

Product Number

1

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

2003-11-14

Regulatory Status

RX

2003
14 Nov
RX Application: 65114

Drug Name

PIPERACILLIN

Product Number

2

Dosage Form

-

Strength

EQ 3GM BASE/VIAL

Approval Date

2003-11-14

65114 / 2

Active Ingredient

PIPERACILLIN SODIUM

Application Number

65114

Product Number

2

Dosage Form

-

Strength

EQ 3GM BASE/VIAL

Approval Date

2003-11-14

Regulatory Status

RX

2003
14 Nov
RX Application: 65114

Drug Name

PIPERACILLIN

Product Number

3

Dosage Form

-

Strength

EQ 4GM BASE/VIAL

Approval Date

2003-11-14

65114 / 3

Active Ingredient

PIPERACILLIN SODIUM

Application Number

65114

Product Number

3

Dosage Form

-

Strength

EQ 4GM BASE/VIAL

Approval Date

2003-11-14

Regulatory Status

RX

2004
12 Jul
RX Application: 65157

Drug Name

PIPERACILLIN

Product Number

1

Dosage Form

-

Strength

EQ 40GM BASE/VIAL

Approval Date

2004-07-12

65157 / 1

Active Ingredient

PIPERACILLIN SODIUM

Application Number

65157

Product Number

1

Dosage Form

-

Strength

EQ 40GM BASE/VIAL

Approval Date

2004-07-12

Regulatory Status

RX

2011
31 May
RX Application: 65523

Drug Name

PIPERACILLIN AND TAZOBACTAM

Product Number

1

Dosage Form

-

Strength

EQ 2GM BASE/VIAL;EQ 250MG BASE/VIAL

Approval Date

2011-05-31

65523 / 1

Active Ingredient

PIPERACILLIN SODIUM; TAZOBACTAM SODIUM

Application Number

65523

Product Number

1

Dosage Form

-

Strength

EQ 2GM BASE/VIAL;EQ 250MG BASE/VIAL

Approval Date

2011-05-31

Regulatory Status

RX

2011
31 May
RX Application: 65523

Drug Name

PIPERACILLIN AND TAZOBACTAM

Product Number

2

Dosage Form

-

Strength

EQ 3GM BASE/VIAL;EQ 375MG BASE/VIAL

Approval Date

2011-05-31

65523 / 2

Active Ingredient

PIPERACILLIN SODIUM; TAZOBACTAM SODIUM

Application Number

65523

Product Number

2

Dosage Form

-

Strength

EQ 3GM BASE/VIAL;EQ 375MG BASE/VIAL

Approval Date

2011-05-31

Regulatory Status

RX

2011
31 May
RX Application: 65523

Drug Name

PIPERACILLIN AND TAZOBACTAM

Product Number

3

Dosage Form

-

Strength

EQ 4GM BASE/VIAL;EQ 500MG BASE/VIAL

Approval Date

2011-05-31

65523 / 3

Active Ingredient

PIPERACILLIN SODIUM; TAZOBACTAM SODIUM

Application Number

65523

Product Number

3

Dosage Form

-

Strength

EQ 4GM BASE/VIAL;EQ 500MG BASE/VIAL

Approval Date

2011-05-31

Regulatory Status

RX

2011
31 May
RX Application: 90498

Drug Name

PIPERACILLIN AND TAZOBACTAM

Product Number

1

Dosage Form

-

Strength

EQ 36GM BASE/VIAL;EQ 4.5GM BASE/VIAL

Approval Date

2011-05-31

90498 / 1

Active Ingredient

PIPERACILLIN SODIUM; TAZOBACTAM SODIUM

Application Number

90498

Product Number

1

Dosage Form

-

Strength

EQ 36GM BASE/VIAL;EQ 4.5GM BASE/VIAL

Approval Date

2011-05-31

Regulatory Status

RX

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Drug Status Breakdown
21 total
  • RX
Official Source

FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.

Visit FDA Orange Book
FDA Approved Drug Record Details Preview

Explore important FDA approved drug information available in the records above.

Drug Name

AMPICILLIN AND SULBACTAM

Application Number

65222

Product Number

1

Active Ingredient

AMPICILLIN SODIUM; SULBACTAM SODIUM

Dosage Form

-

Strength

EQ 1GM BASE/VIAL;EQ 500MG BASE/VIAL

FDA Approved Drug Data

Approved drug product information

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