ACS DOBFAR SPA
FDA Approved Drugs

ACS DOBFAR SPA

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 Discontinued
  • Total Records 63
  • Latest Approval Date Oct 26, 2018
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
63
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Discontinued
32
View
RX
31
View
Company Overview

Company

ACS DOBFAR SPA

Country

Italy

Website

Visit Website

Email

info@acsdobfar.it

Social Profiles

Company Snapshot

ACS DOBFAR SPA

Viale Addetta 4/12 20067 Tribiano (Milan)

Italy

www.acsdobfar.it/ info@acsdobfar.it View on Map
FDA Approved Drug Records ( 63 records )
2009
23 Dec
RX Application: 65403

Drug Name

AMPICILLIN AND SULBACTAM

Product Number

1

Dosage Form

-

Strength

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

Approval Date

2009-12-23

65403 / 1

Active Ingredient

AMPICILLIN SODIUM; SULBACTAM SODIUM

Application Number

65403

Product Number

1

Dosage Form

-

Strength

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

Approval Date

2009-12-23

Regulatory Status

RX

2009
22 Dec
RX Application: 65406

Drug Name

AMPICILLIN AND SULBACTAM

Product Number

1

Dosage Form

-

Strength

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

Approval Date

2009-12-22

65406 / 1

Active Ingredient

AMPICILLIN SODIUM; SULBACTAM SODIUM

Application Number

65406

Product Number

1

Dosage Form

-

Strength

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

Approval Date

2009-12-22

Regulatory Status

RX

2009
22 Dec
RX Application: 65406

Drug Name

AMPICILLIN AND SULBACTAM

Product Number

2

Dosage Form

-

Strength

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

Approval Date

2009-12-22

65406 / 2

Active Ingredient

AMPICILLIN SODIUM; SULBACTAM SODIUM

Application Number

65406

Product Number

2

Dosage Form

-

Strength

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

Approval Date

2009-12-22

Regulatory Status

RX

2013
03 Apr
Discontinued Application: 90884

Drug Name

AMPICILLIN SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

2013-04-03

90884 / 1

Active Ingredient

AMPICILLIN SODIUM

Application Number

90884

Product Number

1

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

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2013-04-03

90884 / 2

Active Ingredient

AMPICILLIN SODIUM

Application Number

90884

Product Number

2

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

3

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

2013-04-03

90884 / 3

Active Ingredient

AMPICILLIN SODIUM

Application Number

90884

Product Number

3

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

2013-04-03

Regulatory Status

Discontinued

2013
03 Apr
RX Application: 90889

Drug Name

AMPICILLIN SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 10GM BASE/VIAL

Approval Date

2013-04-03

90889 / 1

Active Ingredient

AMPICILLIN SODIUM

Application Number

90889

Product Number

1

Dosage Form

-

Strength

EQ 10GM BASE/VIAL

Approval Date

2013-04-03

Regulatory Status

RX

1982
01 Jan
Discontinued Application: 62206

Drug Name

CEFACLOR

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

1982-01-01

62206 / 1

Active Ingredient

CEFACLOR

Application Number

62206

Product Number

1

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

2

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

1982-01-01

62206 / 2

Active Ingredient

CEFACLOR

Application Number

62206

Product Number

2

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

3

Dosage Form

-

Strength

EQ 187MG BASE/5ML

Approval Date

1988-04-20

62206 / 3

Active Ingredient

CEFACLOR

Application Number

62206

Product Number

3

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

4

Dosage Form

-

Strength

EQ 375MG BASE/5ML

Approval Date

1988-04-20

62206 / 4

Active Ingredient

CEFACLOR

Application Number

62206

Product Number

4

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

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1991-12-27

63207 / 1

Active Ingredient

CEFAZOLIN SODIUM

Application Number

63207

Product Number

1

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

1

Dosage Form

-

Strength

EQ 10GM BASE/VIAL

Approval Date

1991-12-27

63209 / 1

Active Ingredient

CEFAZOLIN SODIUM

Application Number

63209

Product Number

1

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

2

Dosage Form

-

Strength

EQ 20GM BASE/VIAL

Approval Date

1999-04-30

63209 / 2

Active Ingredient

CEFAZOLIN SODIUM

Application Number

63209

Product Number

2

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

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1991-12-27

63214 / 1

Active Ingredient

CEFAZOLIN SODIUM

Application Number

63214

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1991-12-27

Regulatory Status

Discontinued

2008
22 Oct
RX Application: 65303

Drug Name

CEFAZOLIN SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

2008-10-22

65303 / 1

Active Ingredient

CEFAZOLIN SODIUM

Application Number

65303

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

2008-10-22

Regulatory Status

RX

2008
22 Oct
RX Application: 65303

Drug Name

CEFAZOLIN SODIUM

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2008-10-22

65303 / 2

Active Ingredient

CEFAZOLIN SODIUM

Application Number

65303

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2008-10-22

Regulatory Status

RX

2008
22 Oct
RX Application: 65306

Drug Name

CEFAZOLIN SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 10GM BASE/VIAL

Approval Date

2008-10-22

65306 / 1

Active Ingredient

CEFAZOLIN SODIUM

Application Number

65306

Product Number

1

Dosage Form

-

Strength

EQ 10GM BASE/VIAL

Approval Date

2008-10-22

Regulatory Status

RX

2014
18 Aug
RX Application: 65306

Drug Name

CEFAZOLIN SODIUM

Product Number

2

Dosage Form

-

Strength

EQ 20GM BASE/VIAL

Approval Date

2014-08-18

65306 / 2

Active Ingredient

CEFAZOLIN SODIUM

Application Number

65306

Product Number

2

Dosage Form

-

Strength

EQ 20GM BASE/VIAL

Approval Date

2014-08-18

Regulatory Status

RX

2008
20 Mar
RX Application: 65441

Drug Name

CEFEPIME HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2008-03-20

65441 / 1

Active Ingredient

CEFEPIME HYDROCHLORIDE

Application Number

65441

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2008-03-20

Regulatory Status

RX

2008
20 Mar
RX Application: 65441

Drug Name

CEFEPIME HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

2008-03-20

65441 / 2

Active Ingredient

CEFEPIME HYDROCHLORIDE

Application Number

65441

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

2008-03-20

Regulatory Status

RX

2009
12 Jun
RX Application: 65414

Drug Name

CEFOXITIN

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2009-06-12

65414 / 1

Active Ingredient

CEFOXITIN SODIUM

Application Number

65414

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2009-06-12

Regulatory Status

RX

2009
12 Jun
RX Application: 65414

Drug Name

CEFOXITIN

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

2009-06-12

65414 / 2

Active Ingredient

CEFOXITIN SODIUM

Application Number

65414

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

2009-06-12

Regulatory Status

RX

2010
19 May
RX Application: 65415

Drug Name

CEFOXITIN

Product Number

1

Dosage Form

-

Strength

EQ 10GM BASE/VIAL

Approval Date

2010-05-19

65415 / 1

Active Ingredient

CEFOXITIN SODIUM

Application Number

65415

Product Number

1

Dosage Form

-

Strength

EQ 10GM BASE/VIAL

Approval Date

2010-05-19

Regulatory Status

RX

2011
31 Aug
Discontinued Application: 65464

Drug Name

CEFOXITIN

Product Number

1

Dosage Form

-

Strength

EQ 10GM BASE/VIAL

Approval Date

2011-08-31

65464 / 1

Active Ingredient

CEFOXITIN SODIUM

Application Number

65464

Product Number

1

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

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2011-08-31

65467 / 1

Active Ingredient

CEFOXITIN SODIUM

Application Number

65467

Product Number

1

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

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

2011-08-31

65467 / 2

Active Ingredient

CEFOXITIN SODIUM

Application Number

65467

Product Number

2

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

1

Dosage Form

-

Strength

500MG/VIAL

Approval Date

1985-11-20

62640 / 1

Active Ingredient

CEFTAZIDIME

Application Number

62640

Product Number

1

Dosage Form

-

Strength

500MG/VIAL

Approval Date

1985-11-20

Regulatory Status

Discontinued

1985
20 Nov
RX Application: 62640

Drug Name

CEFTAZIDIME

Product Number

2

Dosage Form

-

Strength

1GM/VIAL

Approval Date

1985-11-20

62640 / 2

Active Ingredient

CEFTAZIDIME

Application Number

62640

Product Number

2

Dosage Form

-

Strength

1GM/VIAL

Approval Date

1985-11-20

Regulatory Status

RX

1985
20 Nov
RX Application: 62640

Drug Name

CEFTAZIDIME

Product Number

3

Dosage Form

-

Strength

2GM/VIAL

Approval Date

1985-11-20

62640 / 3

Active Ingredient

CEFTAZIDIME

Application Number

62640

Product Number

3

Dosage Form

-

Strength

2GM/VIAL

Approval Date

1985-11-20

Regulatory Status

RX

1992
03 Feb
RX Application: 62640

Drug Name

CEFTAZIDIME

Product Number

4

Dosage Form

-

Strength

6GM/VIAL

Approval Date

1992-02-03

62640 / 4

Active Ingredient

CEFTAZIDIME

Application Number

62640

Product Number

4

Dosage Form

-

Strength

6GM/VIAL

Approval Date

1992-02-03

Regulatory Status

RX

2007
28 Feb
Discontinued Application: 65268

Drug Name

CEFTRIAXONE

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2007-02-28

65268 / 1

Active Ingredient

CEFTRIAXONE SODIUM

Application Number

65268

Product Number

1

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

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

2007-02-28

65268 / 2

Active Ingredient

CEFTRIAXONE SODIUM

Application Number

65268

Product Number

2

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

1

Dosage Form

-

Strength

EQ 10GM BASE/VIAL

Approval Date

2007-02-28

65269 / 1

Active Ingredient

CEFTRIAXONE SODIUM

Application Number

65269

Product Number

1

Dosage Form

-

Strength

EQ 10GM BASE/VIAL

Approval Date

2007-02-28

Regulatory Status

Discontinued

2008
24 Jul
RX Application: 65328

Drug Name

CEFTRIAXONE

Product Number

1

Dosage Form

-

Strength

EQ 10GM BASE/VIAL

Approval Date

2008-07-24

65328 / 1

Active Ingredient

CEFTRIAXONE SODIUM

Application Number

65328

Product Number

1

Dosage Form

-

Strength

EQ 10GM BASE/VIAL

Approval Date

2008-07-24

Regulatory Status

RX

2008
24 Jul
RX Application: 65329

Drug Name

CEFTRIAXONE

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

2008-07-24

65329 / 1

Active Ingredient

CEFTRIAXONE SODIUM

Application Number

65329

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

2008-07-24

Regulatory Status

RX

2008
24 Jul
RX Application: 65329

Drug Name

CEFTRIAXONE

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2008-07-24

65329 / 2

Active Ingredient

CEFTRIAXONE SODIUM

Application Number

65329

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2008-07-24

Regulatory Status

RX

2008
24 Jul
RX Application: 65329

Drug Name

CEFTRIAXONE

Product Number

3

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

2008-07-24

65329 / 3

Active Ingredient

CEFTRIAXONE SODIUM

Application Number

65329

Product Number

3

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

2008-07-24

Regulatory Status

RX

1997
30 May
Discontinued Application: 64124

Drug Name

CEFUROXIME SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 7.5GM BASE/VIAL

Approval Date

1997-05-30

64124 / 1

Active Ingredient

CEFUROXIME SODIUM

Application Number

64124

Product Number

1

Dosage Form

-

Strength

EQ 7.5GM BASE/VIAL

Approval Date

1997-05-30

Regulatory Status

Discontinued

1997
30 May
RX Application: 64125

Drug Name

CEFUROXIME SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 750MG BASE/VIAL

Approval Date

1997-05-30

64125 / 1

Active Ingredient

CEFUROXIME SODIUM

Application Number

64125

Product Number

1

Dosage Form

-

Strength

EQ 750MG BASE/VIAL

Approval Date

1997-05-30

Regulatory Status

RX

1997
30 May
RX Application: 64125

Drug Name

CEFUROXIME SODIUM

Product Number

2

Dosage Form

-

Strength

EQ 1.5GM BASE/VIAL

Approval Date

1997-05-30

64125 / 2

Active Ingredient

CEFUROXIME SODIUM

Application Number

64125

Product Number

2

Dosage Form

-

Strength

EQ 1.5GM BASE/VIAL

Approval Date

1997-05-30

Regulatory Status

RX

1982
01 Jan
Discontinued Application: 62117

Drug Name

CEPHALEXIN

Product Number

1

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

Active Ingredient

CEPHALEXIN

Application Number

62117

Product Number

1

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

2

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

Active Ingredient

CEPHALEXIN

Application Number

62117

Product Number

2

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

3

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

Active Ingredient

CEPHALEXIN

Application Number

62117

Product Number

3

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

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

1982-01-01

62118 / 1

Active Ingredient

CEPHALEXIN

Application Number

62118

Product Number

1

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

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1982-01-01

62118 / 2

Active Ingredient

CEPHALEXIN

Application Number

62118

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

2018
16 Apr
RX Application: 208790

Drug Name

ERTAPENEM SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2018-04-16

208790 / 1

Active Ingredient

ERTAPENEM SODIUM

Application Number

208790

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2018-04-16

Regulatory Status

RX

2011
21 Dec
RX Application: 90577

Drug Name

IMIPENEM AND CILASTATIN

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE/VIAL;250MG/VIAL

Approval Date

2011-12-21

90577 / 1

Active Ingredient

CILASTATIN SODIUM; IMIPENEM

Application Number

90577

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE/VIAL;250MG/VIAL

Approval Date

2011-12-21

Regulatory Status

RX

2011
21 Dec
RX Application: 90577

Drug Name

IMIPENEM AND CILASTATIN

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE/VIAL;500MG/VIAL

Approval Date

2011-12-21

90577 / 2

Active Ingredient

CILASTATIN SODIUM; IMIPENEM

Application Number

90577

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE/VIAL;500MG/VIAL

Approval Date

2011-12-21

Regulatory Status

RX

1986
10 Jan
Discontinued Application: 62591

Drug Name

KEFUROX

Product Number

1

Dosage Form

-

Strength

EQ 750MG BASE/VIAL

Approval Date

1986-01-10

62591 / 1

Active Ingredient

CEFUROXIME SODIUM

Application Number

62591

Product Number

1

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

2

Dosage Form

-

Strength

EQ 1.5GM BASE/VIAL

Approval Date

1986-01-10

62591 / 2

Active Ingredient

CEFUROXIME SODIUM

Application Number

62591

Product Number

2

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

3

Dosage Form

-

Strength

EQ 7.5GM BASE/VIAL

Approval Date

1987-12-17

62591 / 3

Active Ingredient

CEFUROXIME SODIUM

Application Number

62591

Product Number

3

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

1

Dosage Form

-

Strength

EQ 250MG BASE/VIAL

Approval Date

1982-01-01

61773 / 1

Active Ingredient

CEFAZOLIN SODIUM

Application Number

61773

Product Number

1

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

2

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

1982-01-01

61773 / 2

Active Ingredient

CEFAZOLIN SODIUM

Application Number

61773

Product Number

2

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

3

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

1982-01-01

61773 / 3

Active Ingredient

CEFAZOLIN SODIUM

Application Number

61773

Product Number

3

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

4

Dosage Form

-

Strength

EQ 10GM BASE/VIAL

Approval Date

1982-01-01

61773 / 4

Active Ingredient

CEFAZOLIN SODIUM

Application Number

61773

Product Number

4

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

5

Dosage Form

-

Strength

EQ 20GM BASE/VIAL

Approval Date

1987-09-08

61773 / 5

Active Ingredient

CEFAZOLIN SODIUM

Application Number

61773

Product Number

5

Dosage Form

-

Strength

EQ 20GM BASE/VIAL

Approval Date

1987-09-08

Regulatory Status

Discontinued

2011
26 Oct
RX Application: 91404

Drug Name

MEROPENEM

Product Number

1

Dosage Form

-

Strength

500MG/VIAL

Approval Date

2011-10-26

91404 / 1

Active Ingredient

MEROPENEM

Application Number

91404

Product Number

1

Dosage Form

-

Strength

500MG/VIAL

Approval Date

2011-10-26

Regulatory Status

RX

2011
26 Oct
RX Application: 91404

Drug Name

MEROPENEM

Product Number

2

Dosage Form

-

Strength

1GM/VIAL

Approval Date

2011-10-26

91404 / 2

Active Ingredient

MEROPENEM

Application Number

91404

Product Number

2

Dosage Form

-

Strength

1GM/VIAL

Approval Date

2011-10-26

Regulatory Status

RX

2016
09 Jun
RX Application: 204139

Drug Name

MEROPENEM

Product Number

1

Dosage Form

-

Strength

500MG/VIAL

Approval Date

2016-06-09

204139 / 1

Active Ingredient

MEROPENEM

Application Number

204139

Product Number

1

Dosage Form

-

Strength

500MG/VIAL

Approval Date

2016-06-09

Regulatory Status

RX

2016
09 Jun
RX Application: 204139

Drug Name

MEROPENEM

Product Number

2

Dosage Form

-

Strength

1GM/VIAL

Approval Date

2016-06-09

204139 / 2

Active Ingredient

MEROPENEM

Application Number

204139

Product Number

2

Dosage Form

-

Strength

1GM/VIAL

Approval Date

2016-06-09

Regulatory Status

RX

2018
26 Oct
RX Application: 205043

Drug Name

PENICILLIN G POTASSIUM

Product Number

1

Dosage Form

-

Strength

5,000,000 UNITS/VIAL

Approval Date

2018-10-26

205043 / 1

Active Ingredient

PENICILLIN G POTASSIUM

Application Number

205043

Product Number

1

Dosage Form

-

Strength

5,000,000 UNITS/VIAL

Approval Date

2018-10-26

Regulatory Status

RX

2018
26 Oct
RX Application: 205043

Drug Name

PENICILLIN G POTASSIUM

Product Number

2

Dosage Form

-

Strength

20,000,000 UNITS/VIAL

Approval Date

2018-10-26

205043 / 2

Active Ingredient

PENICILLIN G POTASSIUM

Application Number

205043

Product Number

2

Dosage Form

-

Strength

20,000,000 UNITS/VIAL

Approval Date

2018-10-26

Regulatory Status

RX

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Drug Status Breakdown
63 total
  • RX
  • Discontinued
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

65403

Product Number

1

Active Ingredient

AMPICILLIN SODIUM; SULBACTAM SODIUM

Dosage Form

-

Strength

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

FDA Approved Drug Data

Approved drug product information

Regular Updates

Data maintained from official sources

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Searchable pharmaceutical data

Reliable Data

Organized FDA drug records

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