Istituto Biochimico Italiano Giovanni Lorenzini SpA Discontinued
FDA Approved Drugs

Istituto Biochimico Italiano Giovanni Lorenzini SpA Discontinued

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.

Discontinued
  • Total Records 6
  • Latest Approval Date Dec 11, 1995
  • Data Source FDA
  • First Approval Date Jul 12, 1993
All
27
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Discontinued
6
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RX
21
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Company Overview

Company

Istituto Biochimico Italiano Giovanni Lorenzini SpA Discontinued

Country

Italy

Website

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Email

 info@ibi-lorenzini.com

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Company Snapshot

Istituto Biochimico Italiano Giovanni Lorenzini SpA Discontinued

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 ( 6 records )
1993
12 Jul
Discontinued Application: 62797

Drug Name

AMPICILLIN SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/VIAL

Approval Date

1993-07-12

62797 / 1

Active Ingredient

AMPICILLIN SODIUM

Application Number

62797

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/VIAL

Approval Date

1993-07-12

Regulatory Status

Discontinued

1995
11 Dec
Discontinued Application: 62798

Drug Name

OXACILLIN SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1995-12-11

62798 / 1

Active Ingredient

OXACILLIN SODIUM

Application Number

62798

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1995-12-11

Regulatory Status

Discontinued

1995
11 Dec
Discontinued Application: 62798

Drug Name

OXACILLIN SODIUM

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

1995-12-11

62798 / 2

Active Ingredient

OXACILLIN SODIUM

Application Number

62798

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

1995-12-11

Regulatory Status

Discontinued

1995
11 Dec
Discontinued Application: 62798

Drug Name

OXACILLIN SODIUM

Product Number

3

Dosage Form

-

Strength

EQ 125MG BASE/VIAL

Approval Date

1995-12-11

62798 / 3

Active Ingredient

OXACILLIN SODIUM

Application Number

62798

Product Number

3

Dosage Form

-

Strength

EQ 125MG BASE/VIAL

Approval Date

1995-12-11

Regulatory Status

Discontinued

1995
11 Dec
Discontinued Application: 62798

Drug Name

OXACILLIN SODIUM

Product Number

4

Dosage Form

-

Strength

EQ 250MG BASE/VIAL

Approval Date

1995-12-11

62798 / 4

Active Ingredient

OXACILLIN SODIUM

Application Number

62798

Product Number

4

Dosage Form

-

Strength

EQ 250MG BASE/VIAL

Approval Date

1995-12-11

Regulatory Status

Discontinued

1995
11 Dec
Discontinued Application: 62798

Drug Name

OXACILLIN SODIUM

Product Number

5

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1995-12-11

62798 / 5

Active Ingredient

OXACILLIN SODIUM

Application Number

62798

Product Number

5

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1995-12-11

Regulatory Status

Discontinued

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Drug Status Breakdown
6 total
  • Discontinued
Official Source

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

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

Drug Name

AMPICILLIN SODIUM

Application Number

62797

Product Number

1

Active Ingredient

AMPICILLIN SODIUM

Dosage Form

-

Strength

EQ 125MG BASE/VIAL

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