ACS DOBFAR SPA Discontinued
FDA Approved Drugs

ACS DOBFAR 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 32
Latest Approval Date Apr 03, 2013
Data Source FDA
First Approval Date Jan 01, 1982

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Company Overview

Company

ACS DOBFAR SPA Discontinued

Country

Italy

Website

Visit Website

info@acsdobfar.it

Social Profiles

Company Snapshot

ACS DOBFAR SPA Discontinued

Viale Addetta 4/12 20067 Tribiano (Milan)

Italy

www.acsdobfar.it/ info@acsdobfar.it View on Map

FDA Approved Drug Records ( 32 records )

2013

03 Apr

Discontinued Application: 90884

Drug Name

AMPICILLIN SODIUM

Product Number

Dosage Form

Strength

EQ 500MG BASE/VIAL

Approval Date

2013-04-03

90884 / 1 View Details

Active Ingredient

AMPICILLIN SODIUM

Application Number

90884

Product Number

Dosage Form

Strength

EQ 500MG BASE/VIAL

Approval Date

2013-04-03

Regulatory Status

Discontinued

2013

03 Apr

Discontinued Application: 90884

Drug Name

AMPICILLIN SODIUM

Product Number

Dosage Form

Strength

EQ 1GM BASE/VIAL

Approval Date

2013-04-03

90884 / 2 View Details

Active Ingredient

AMPICILLIN SODIUM

Application Number

90884

Product Number

Dosage Form

Strength

EQ 1GM BASE/VIAL

Approval Date

2013-04-03

Regulatory Status

Discontinued

2013

03 Apr

Discontinued Application: 90884

Drug Name

AMPICILLIN SODIUM

Product Number

Dosage Form

Strength

EQ 2GM BASE/VIAL

Approval Date

2013-04-03

90884 / 3 View Details

Active Ingredient

AMPICILLIN SODIUM

Application Number

90884

Product Number

Dosage Form

Strength

EQ 2GM BASE/VIAL

Approval Date

2013-04-03

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 62206

Drug Name

CEFACLOR

Product Number

Dosage Form

Strength

EQ 125MG BASE/5ML

Approval Date

1982-01-01

62206 / 1 View Details

Active Ingredient

CEFACLOR

Application Number

62206

Product Number

Dosage Form

Strength

EQ 125MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 62206

Drug Name

CEFACLOR

Product Number

Dosage Form

Strength

EQ 250MG BASE/5ML

Approval Date

1982-01-01

62206 / 2 View Details

Active Ingredient

CEFACLOR

Application Number

62206

Product Number

Dosage Form

Strength

EQ 250MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1988

20 Apr

Discontinued Application: 62206

Drug Name

CEFACLOR

Product Number

Dosage Form

Strength

EQ 187MG BASE/5ML

Approval Date

1988-04-20

62206 / 3 View Details

Active Ingredient

CEFACLOR

Application Number

62206

Product Number

Dosage Form

Strength

EQ 187MG BASE/5ML

Approval Date

1988-04-20

Regulatory Status

Discontinued

1988

20 Apr

Discontinued Application: 62206

Drug Name

CEFACLOR

Product Number

Dosage Form

Strength

EQ 375MG BASE/5ML

Approval Date

1988-04-20

62206 / 4 View Details

Active Ingredient

CEFACLOR

Application Number

62206

Product Number

Dosage Form

Strength

EQ 375MG BASE/5ML

Approval Date

1988-04-20

Regulatory Status

Discontinued

1991

27 Dec

Discontinued Application: 63207

Drug Name

CEFAZOLIN SODIUM

Product Number

Dosage Form

Strength

EQ 1GM BASE/VIAL

Approval Date

1991-12-27

63207 / 1 View Details

Active Ingredient

CEFAZOLIN SODIUM

Application Number

63207

Product Number

Dosage Form

Strength

EQ 1GM BASE/VIAL

Approval Date

1991-12-27

Regulatory Status

Discontinued

1991

27 Dec

Discontinued Application: 63209

Drug Name

CEFAZOLIN SODIUM

Product Number

Dosage Form

Strength

EQ 10GM BASE/VIAL

Approval Date

1991-12-27

63209 / 1 View Details

Active Ingredient

CEFAZOLIN SODIUM

Application Number

63209

Product Number

Dosage Form

Strength

EQ 10GM BASE/VIAL

Approval Date

1991-12-27

Regulatory Status

Discontinued

1999

30 Apr

Discontinued Application: 63209

Drug Name

CEFAZOLIN SODIUM

Product Number

Dosage Form

Strength

EQ 20GM BASE/VIAL

Approval Date

1999-04-30

63209 / 2 View Details

Active Ingredient

CEFAZOLIN SODIUM

Application Number

63209

Product Number

Dosage Form

Strength

EQ 20GM BASE/VIAL

Approval Date

1999-04-30

Regulatory Status

Discontinued

1991

27 Dec

Discontinued Application: 63214

Drug Name

CEFAZOLIN SODIUM

Product Number

Dosage Form

Strength

EQ 500MG BASE/VIAL

Approval Date

1991-12-27

63214 / 1 View Details

Active Ingredient

CEFAZOLIN SODIUM

Application Number

63214

Product Number

Dosage Form

Strength

EQ 500MG BASE/VIAL

Approval Date

1991-12-27

Regulatory Status

Discontinued

2011

31 Aug

Discontinued Application: 65464

Drug Name

CEFOXITIN

Product Number

Dosage Form

Strength

EQ 10GM BASE/VIAL

Approval Date

2011-08-31

65464 / 1 View Details

Active Ingredient

CEFOXITIN SODIUM

Application Number

65464

Product Number

Dosage Form

Strength

EQ 10GM BASE/VIAL

Approval Date

2011-08-31

Regulatory Status

Discontinued

2011

31 Aug

Discontinued Application: 65467

Drug Name

CEFOXITIN

Product Number

Dosage Form

Strength

EQ 1GM BASE/VIAL

Approval Date

2011-08-31

65467 / 1 View Details

Active Ingredient

CEFOXITIN SODIUM

Application Number

65467

Product Number

Dosage Form

Strength

EQ 1GM BASE/VIAL

Approval Date

2011-08-31

Regulatory Status

Discontinued

2011

31 Aug

Discontinued Application: 65467

Drug Name

CEFOXITIN

Product Number

Dosage Form

Strength

EQ 2GM BASE/VIAL

Approval Date

2011-08-31

65467 / 2 View Details

Active Ingredient

CEFOXITIN SODIUM

Application Number

65467

Product Number

Dosage Form

Strength

EQ 2GM BASE/VIAL

Approval Date

2011-08-31

Regulatory Status

Discontinued

1985

20 Nov

Discontinued Application: 62640

Drug Name

CEFTAZIDIME

Product Number

Dosage Form

Strength

500MG/VIAL

Approval Date

1985-11-20

62640 / 1 View Details

Active Ingredient

CEFTAZIDIME

Application Number

62640

Product Number

Dosage Form

Strength

500MG/VIAL

Approval Date

1985-11-20

Regulatory Status

Discontinued

2007

28 Feb

Discontinued Application: 65268

Drug Name

CEFTRIAXONE

Product Number

Dosage Form

Strength

EQ 1GM BASE/VIAL

Approval Date

2007-02-28

65268 / 1 View Details

Active Ingredient

CEFTRIAXONE SODIUM

Application Number

65268

Product Number

Dosage Form

Strength

EQ 1GM BASE/VIAL

Approval Date

2007-02-28

Regulatory Status

Discontinued

2007

28 Feb

Discontinued Application: 65268

Drug Name

CEFTRIAXONE

Product Number

Dosage Form

Strength

EQ 2GM BASE/VIAL

Approval Date

2007-02-28

65268 / 2 View Details

Active Ingredient

CEFTRIAXONE SODIUM

Application Number

65268

Product Number

Dosage Form

Strength

EQ 2GM BASE/VIAL

Approval Date

2007-02-28

Regulatory Status

Discontinued

2007

28 Feb

Discontinued Application: 65269

Drug Name

CEFTRIAXONE

Product Number

Dosage Form

Strength

EQ 10GM BASE/VIAL

Approval Date

2007-02-28

65269 / 1 View Details

Active Ingredient

CEFTRIAXONE SODIUM

Application Number

65269

Product Number

Dosage Form

Strength

EQ 10GM BASE/VIAL

Approval Date

2007-02-28

Regulatory Status

Discontinued

1997

30 May

Discontinued Application: 64124

Drug Name

CEFUROXIME SODIUM

Product Number

Dosage Form

Strength

EQ 7.5GM BASE/VIAL

Approval Date

1997-05-30

64124 / 1 View Details

Active Ingredient

CEFUROXIME SODIUM

Application Number

64124

Product Number

Dosage Form

Strength

EQ 7.5GM BASE/VIAL

Approval Date

1997-05-30

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 62117

Drug Name

CEPHALEXIN

Product Number

Dosage Form

Strength

EQ 100MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons*

Approval Date

1982-01-01

62117 / 1 View Details

Active Ingredient

CEPHALEXIN

Application Number

62117

Product Number

Dosage Form

Strength

EQ 100MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons*

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 62117

Drug Name

CEPHALEXIN

Product Number

Dosage Form

Strength

EQ 125MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons*

Approval Date

1982-01-01

62117 / 2 View Details

Active Ingredient

CEPHALEXIN

Application Number

62117

Product Number

Dosage Form

Strength

EQ 125MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons*

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 62117

Drug Name

CEPHALEXIN

Product Number

Dosage Form

Strength

EQ 250MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons*

Approval Date

1982-01-01

62117 / 3 View Details

Active Ingredient

CEPHALEXIN

Application Number

62117

Product Number

Dosage Form

Strength

EQ 250MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons*

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 62118

Drug Name

CEPHALEXIN

Product Number

Dosage Form

Strength

EQ 250MG BASE

Approval Date

1982-01-01

62118 / 1 View Details

Active Ingredient

CEPHALEXIN

Application Number

62118

Product Number

Dosage Form

Strength

EQ 250MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 62118

Drug Name

CEPHALEXIN

Product Number

Dosage Form

Strength

EQ 500MG BASE

Approval Date

1982-01-01

62118 / 2 View Details

Active Ingredient

CEPHALEXIN

Application Number

62118

Product Number

Dosage Form

Strength

EQ 500MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1986

10 Jan

Discontinued Application: 62591

Drug Name

KEFUROX

Product Number

Dosage Form

Strength

EQ 750MG BASE/VIAL

Approval Date

1986-01-10

62591 / 1 View Details

Active Ingredient

CEFUROXIME SODIUM

Application Number

62591

Product Number

Dosage Form

Strength

EQ 750MG BASE/VIAL

Approval Date

1986-01-10

Regulatory Status

Discontinued

1986

10 Jan

Discontinued Application: 62591

Drug Name

KEFUROX

Product Number

Dosage Form

Strength

EQ 1.5GM BASE/VIAL

Approval Date

1986-01-10

62591 / 2 View Details

Active Ingredient

CEFUROXIME SODIUM

Application Number

62591

Product Number

Dosage Form

Strength

EQ 1.5GM BASE/VIAL

Approval Date

1986-01-10

Regulatory Status

Discontinued

1987

17 Dec

Discontinued Application: 62591

Drug Name

KEFUROX

Product Number

Dosage Form

Strength

EQ 7.5GM BASE/VIAL

Approval Date

1987-12-17

62591 / 3 View Details

Active Ingredient

CEFUROXIME SODIUM

Application Number

62591

Product Number

Dosage Form

Strength

EQ 7.5GM BASE/VIAL

Approval Date

1987-12-17

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 61773

Drug Name

KEFZOL

Product Number

Dosage Form

Strength

EQ 250MG BASE/VIAL

Approval Date

1982-01-01

61773 / 1 View Details

Active Ingredient

CEFAZOLIN SODIUM

Application Number

61773

Product Number

Dosage Form

Strength

EQ 250MG BASE/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 61773

Drug Name

KEFZOL

Product Number

Dosage Form

Strength

EQ 500MG BASE/VIAL

Approval Date

1982-01-01

61773 / 2 View Details

Active Ingredient

CEFAZOLIN SODIUM

Application Number

61773

Product Number

Dosage Form

Strength

EQ 500MG BASE/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 61773

Drug Name

KEFZOL

Product Number

Dosage Form

Strength

EQ 1GM BASE/VIAL

Approval Date

1982-01-01

61773 / 3 View Details

Active Ingredient

CEFAZOLIN SODIUM

Application Number

61773

Product Number

Dosage Form

Strength

EQ 1GM BASE/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982

01 Jan

Discontinued Application: 61773

Drug Name

KEFZOL

Product Number

Dosage Form

Strength

EQ 10GM BASE/VIAL

Approval Date

1982-01-01

61773 / 4 View Details

Active Ingredient

CEFAZOLIN SODIUM

Application Number

61773

Product Number

Dosage Form

Strength

EQ 10GM BASE/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1987

08 Sep

Discontinued Application: 61773

Drug Name

KEFZOL

Product Number

Dosage Form

Strength

EQ 20GM BASE/VIAL

Approval Date

1987-09-08

61773 / 5 View Details

Active Ingredient

CEFAZOLIN SODIUM

Application Number

61773

Product Number

Dosage Form

Strength

EQ 20GM BASE/VIAL

Approval Date

1987-09-08

Regulatory Status

Discontinued

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Drug Status Breakdown

32 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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Drug Name

AMPICILLIN SODIUM

Application Number

90884

Product Number

Active Ingredient

AMPICILLIN SODIUM

Dosage Form

Strength

EQ 500MG BASE/VIAL

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

Structured Database

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