Mallinckrodt Pharmaceuticals Discontinued
FDA Approved Drugs

Mallinckrodt Pharmaceuticals 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 121
  • Latest Approval Date Jul 28, 2021
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
244
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Unclassified
4
View
Discontinued
121
View
RX
119
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Company Overview

Company

Mallinckrodt Pharmaceuticals Discontinued

Country

Ireland

Website

Visit Website

Email

simon.plevin@mnk.com

Social Profiles

LinkedIn X / Twitter
Company Snapshot

Mallinckrodt Pharmaceuticals Discontinued

College Business & Technology Park Cruiserath, Blanchardstown Dublin 15

Ireland

www.mallinckrodt.com/ simon.plevin@mnk.com View on Map
FDA Approved Drug Records ( 121 records )
2002
31 Oct
Discontinued Application: 40468

Drug Name

ANEXSIA

Product Number

1

Dosage Form

-

Strength

750MG;10MG

Approval Date

2002-10-31

40468 / 1

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40468

Product Number

1

Dosage Form

-

Strength

750MG;10MG

Approval Date

2002-10-31

Regulatory Status

Discontinued

1987
23 Apr
Discontinued Application: 89160

Drug Name

ANEXSIA

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

1987-04-23

89160 / 1

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

89160

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

1987-04-23

Regulatory Status

Discontinued

1987
30 Sep
Discontinued Application: 89725

Drug Name

ANEXSIA 7.5/650

Product Number

1

Dosage Form

-

Strength

650MG;7.5MG

Approval Date

1987-09-30

89725 / 1

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

89725

Product Number

1

Dosage Form

-

Strength

650MG;7.5MG

Approval Date

1987-09-30

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 13319

Drug Name

ANGIO-CONRAY

Product Number

1

Dosage Form

-

Strength

80%

Approval Date

1982-01-01

13319 / 1

Active Ingredient

IOTHALAMATE SODIUM

Application Number

13319

Product Number

1

Dosage Form

-

Strength

80%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1985
07 Aug
Discontinued Application: 18509

Drug Name

BAROS

Product Number

1

Dosage Form

-

Strength

460MG/GM;420MG/GM

Approval Date

1985-08-07

18509 / 1

Active Ingredient

SODIUM BICARBONATE; TARTARIC ACID

Application Number

18509

Product Number

1

Dosage Form

-

Strength

460MG/GM;420MG/GM

Approval Date

1985-08-07

Regulatory Status

Discontinued

2007
25 Apr
Discontinued Application: 40773

Drug Name

BENZPHETAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

2007-04-25

40773 / 1

Active Ingredient

BENZPHETAMINE HYDROCHLORIDE

Application Number

40773

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

2007-04-25

Regulatory Status

Discontinued

1985
28 Jun
Discontinued Application: 88991

Drug Name

BUCET

Product Number

1

Dosage Form

-

Strength

650MG;50MG

Approval Date

1985-06-28

88991 / 1

Active Ingredient

ACETAMINOPHEN; BUTALBITAL

Application Number

88991

Product Number

1

Dosage Form

-

Strength

650MG;50MG

Approval Date

1985-06-28

Regulatory Status

Discontinued

1985
24 Jan
Discontinued Application: 87804

Drug Name

BUTALBITAL, ACETAMINOPHEN AND CAFFEINE

Product Number

1

Dosage Form

-

Strength

325MG;50MG;40MG

Approval Date

1985-01-24

87804 / 1

Active Ingredient

ACETAMINOPHEN; BUTALBITAL; CAFFEINE

Application Number

87804

Product Number

1

Dosage Form

-

Strength

325MG;50MG;40MG

Approval Date

1985-01-24

Regulatory Status

Discontinued

1985
18 Jul
Discontinued Application: 88743

Drug Name

BUTALBITAL, ACETAMINOPHEN AND CAFFEINE

Product Number

1

Dosage Form

-

Strength

325MG;50MG;40MG

Approval Date

1985-07-18

88743 / 1

Active Ingredient

ACETAMINOPHEN; BUTALBITAL; CAFFEINE

Application Number

88743

Product Number

1

Dosage Form

-

Strength

325MG;50MG;40MG

Approval Date

1985-07-18

Regulatory Status

Discontinued

1985
27 Mar
Discontinued Application: 88758

Drug Name

BUTALBITAL, ACETAMINOPHEN AND CAFFEINE

Product Number

1

Dosage Form

-

Strength

325MG;50MG;40MG

Approval Date

1985-03-27

88758 / 1

Active Ingredient

ACETAMINOPHEN; BUTALBITAL; CAFFEINE

Application Number

88758

Product Number

1

Dosage Form

-

Strength

325MG;50MG;40MG

Approval Date

1985-03-27

Regulatory Status

Discontinued

1985
27 Mar
Discontinued Application: 88765

Drug Name

BUTALBITAL, ACETAMINOPHEN AND CAFFEINE

Product Number

1

Dosage Form

-

Strength

325MG;50MG;40MG

Approval Date

1985-03-27

88765 / 1

Active Ingredient

ACETAMINOPHEN; BUTALBITAL; CAFFEINE

Application Number

88765

Product Number

1

Dosage Form

-

Strength

325MG;50MG;40MG

Approval Date

1985-03-27

Regulatory Status

Discontinued

1985
19 Apr
Discontinued Application: 89067

Drug Name

BUTALBITAL, ACETAMINOPHEN AND CAFFEINE

Product Number

1

Dosage Form

-

Strength

325MG;50MG;40MG

Approval Date

1985-04-19

89067 / 1

Active Ingredient

ACETAMINOPHEN; BUTALBITAL; CAFFEINE

Application Number

89067

Product Number

1

Dosage Form

-

Strength

325MG;50MG;40MG

Approval Date

1985-04-19

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17129

Drug Name

CHOLEBRINE

Product Number

1

Dosage Form

-

Strength

750MG

Approval Date

1982-01-01

17129 / 1

Active Ingredient

IOCETAMIC ACID

Application Number

17129

Product Number

1

Dosage Form

-

Strength

750MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1985
25 Apr
Discontinued Application: 18793

Drug Name

COLD CAPSULE IV

Product Number

1

Dosage Form

-

Strength

12MG;75MG

Approval Date

1985-04-25

18793 / 1

Active Ingredient

CHLORPHENIRAMINE MALEATE; PHENYLPROPANOLAMINE HYDROCHLORIDE

Application Number

18793

Product Number

1

Dosage Form

-

Strength

12MG;75MG

Approval Date

1985-04-25

Regulatory Status

Discontinued

1985
23 Apr
Discontinued Application: 18794

Drug Name

COLD CAPSULE V

Product Number

1

Dosage Form

-

Strength

8MG;75MG

Approval Date

1985-04-23

18794 / 1

Active Ingredient

CHLORPHENIRAMINE MALEATE; PHENYLPROPANOLAMINE HYDROCHLORIDE

Application Number

18794

Product Number

1

Dosage Form

-

Strength

8MG;75MG

Approval Date

1985-04-23

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17685

Drug Name

CONRAY 325

Product Number

1

Dosage Form

-

Strength

54.3%

Approval Date

1982-01-01

17685 / 1

Active Ingredient

IOTHALAMATE SODIUM

Application Number

17685

Product Number

1

Dosage Form

-

Strength

54.3%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 14295

Drug Name

CONRAY 400

Product Number

1

Dosage Form

-

Strength

66.8%

Approval Date

1982-01-01

14295 / 1

Active Ingredient

IOTHALAMATE SODIUM

Application Number

14295

Product Number

1

Dosage Form

-

Strength

66.8%

Approval Date

1982-01-01

Regulatory Status

Discontinued

2010
01 Mar
Discontinued Application: 21217

Drug Name

EXALGO

Product Number

1

Dosage Form

-

Strength

8MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2010-03-01

21217 / 1

Active Ingredient

HYDROMORPHONE HYDROCHLORIDE

Application Number

21217

Product Number

1

Dosage Form

-

Strength

8MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2010-03-01

Regulatory Status

Discontinued

2010
01 Mar
Discontinued Application: 21217

Drug Name

EXALGO

Product Number

2

Dosage Form

-

Strength

12MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2010-03-01

21217 / 2

Active Ingredient

HYDROMORPHONE HYDROCHLORIDE

Application Number

21217

Product Number

2

Dosage Form

-

Strength

12MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2010-03-01

Regulatory Status

Discontinued

2010
01 Mar
Discontinued Application: 21217

Drug Name

EXALGO

Product Number

3

Dosage Form

-

Strength

16MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2010-03-01

21217 / 3

Active Ingredient

HYDROMORPHONE HYDROCHLORIDE

Application Number

21217

Product Number

3

Dosage Form

-

Strength

16MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2010-03-01

Regulatory Status

Discontinued

2012
24 Aug
Discontinued Application: 21217

Drug Name

EXALGO

Product Number

4

Dosage Form

-

Strength

32MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2012-08-24

21217 / 4

Active Ingredient

HYDROMORPHONE HYDROCHLORIDE

Application Number

21217

Product Number

4

Dosage Form

-

Strength

32MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2012-08-24

Regulatory Status

Discontinued

1985
19 Jun
Discontinued Application: 89102

Drug Name

FEMCET

Product Number

1

Dosage Form

-

Strength

325MG;50MG;40MG

Approval Date

1985-06-19

89102 / 1

Active Ingredient

ACETAMINOPHEN; BUTALBITAL; CAFFEINE

Application Number

89102

Product Number

1

Dosage Form

-

Strength

325MG;50MG;40MG

Approval Date

1985-06-19

Regulatory Status

Discontinued

2009
30 Oct
Discontinued Application: 78907

Drug Name

FENTANYL CITRATE

Product Number

1

Dosage Form

-

Strength

EQ 0.2MG BASE

Approval Date

2009-10-30

78907 / 1

Active Ingredient

FENTANYL CITRATE

Application Number

78907

Product Number

1

Dosage Form

-

Strength

EQ 0.2MG BASE

Approval Date

2009-10-30

Regulatory Status

Discontinued

2009
30 Oct
Discontinued Application: 78907

Drug Name

FENTANYL CITRATE

Product Number

2

Dosage Form

-

Strength

EQ 0.4MG BASE

Approval Date

2009-10-30

78907 / 2

Active Ingredient

FENTANYL CITRATE

Application Number

78907

Product Number

2

Dosage Form

-

Strength

EQ 0.4MG BASE

Approval Date

2009-10-30

Regulatory Status

Discontinued

2009
30 Oct
Discontinued Application: 78907

Drug Name

FENTANYL CITRATE

Product Number

3

Dosage Form

-

Strength

EQ 0.6MG BASE

Approval Date

2009-10-30

78907 / 3

Active Ingredient

FENTANYL CITRATE

Application Number

78907

Product Number

3

Dosage Form

-

Strength

EQ 0.6MG BASE

Approval Date

2009-10-30

Regulatory Status

Discontinued

2009
30 Oct
Discontinued Application: 78907

Drug Name

FENTANYL CITRATE

Product Number

4

Dosage Form

-

Strength

EQ 0.8MG BASE

Approval Date

2009-10-30

78907 / 4

Active Ingredient

FENTANYL CITRATE

Application Number

78907

Product Number

4

Dosage Form

-

Strength

EQ 0.8MG BASE

Approval Date

2009-10-30

Regulatory Status

Discontinued

2009
30 Oct
Discontinued Application: 78907

Drug Name

FENTANYL CITRATE

Product Number

5

Dosage Form

-

Strength

EQ 1.2MG BASE

Approval Date

2009-10-30

78907 / 5

Active Ingredient

FENTANYL CITRATE

Application Number

78907

Product Number

5

Dosage Form

-

Strength

EQ 1.2MG BASE

Approval Date

2009-10-30

Regulatory Status

Discontinued

2009
30 Oct
Discontinued Application: 78907

Drug Name

FENTANYL CITRATE

Product Number

6

Dosage Form

-

Strength

EQ 1.6MG BASE

Approval Date

2009-10-30

78907 / 6

Active Ingredient

FENTANYL CITRATE

Application Number

78907

Product Number

6

Dosage Form

-

Strength

EQ 1.6MG BASE

Approval Date

2009-10-30

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 16729

Drug Name

FERROUS CITRATE FE 59

Product Number

1

Dosage Form

-

Strength

25uCi/ML

Approval Date

1982-01-01

16729 / 1

Active Ingredient

FERROUS CITRATE, FE-59

Application Number

16729

Product Number

1

Dosage Form

-

Strength

25uCi/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

2002
29 Jan
Discontinued Application: 75658

Drug Name

FLUOXETINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2002-01-29

75658 / 1

Active Ingredient

FLUOXETINE HYDROCHLORIDE

Application Number

75658

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2002-01-29

Regulatory Status

Discontinued

2002
29 Jan
Discontinued Application: 75658

Drug Name

FLUOXETINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2002-01-29

75658 / 2

Active Ingredient

FLUOXETINE HYDROCHLORIDE

Application Number

75658

Product Number

2

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2002-01-29

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 16666

Drug Name

HIPPURAN I 131

Product Number

1

Dosage Form

-

Strength

0.25mCi/ML

Approval Date

1982-01-01

16666 / 1

Active Ingredient

IODOHIPPURATE SODIUM I-131

Application Number

16666

Product Number

1

Dosage Form

-

Strength

0.25mCi/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1995
01 Jun
Discontinued Application: 40084

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

750MG;7.5MG

Approval Date

1995-06-01

40084 / 1

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40084

Product Number

1

Dosage Form

-

Strength

750MG;7.5MG

Approval Date

1995-06-01

Regulatory Status

Discontinued

1995
01 Jun
Discontinued Application: 40084

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

2

Dosage Form

-

Strength

500MG;5MG

Approval Date

1995-06-01

40084 / 2

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40084

Product Number

2

Dosage Form

-

Strength

500MG;5MG

Approval Date

1995-06-01

Regulatory Status

Discontinued

1996
29 Jul
Discontinued Application: 40084

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

3

Dosage Form

-

Strength

660MG;10MG

Approval Date

1996-07-29

40084 / 3

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40084

Product Number

3

Dosage Form

-

Strength

660MG;10MG

Approval Date

1996-07-29

Regulatory Status

Discontinued

1996
16 Oct
Discontinued Application: 40084

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

4

Dosage Form

-

Strength

650MG;10MG

Approval Date

1996-10-16

40084 / 4

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40084

Product Number

4

Dosage Form

-

Strength

650MG;10MG

Approval Date

1996-10-16

Regulatory Status

Discontinued

1998
27 Feb
Discontinued Application: 40201

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

500MG;7.5MG

Approval Date

1998-02-27

40201 / 1

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40201

Product Number

1

Dosage Form

-

Strength

500MG;7.5MG

Approval Date

1998-02-27

Regulatory Status

Discontinued

1998
27 Feb
Discontinued Application: 40201

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

2

Dosage Form

-

Strength

500MG;10MG

Approval Date

1998-02-27

40201 / 2

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40201

Product Number

2

Dosage Form

-

Strength

500MG;10MG

Approval Date

1998-02-27

Regulatory Status

Discontinued

2001
27 Jun
Discontinued Application: 40418

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

500MG/15ML;7.5MG/15ML

Approval Date

2001-06-27

40418 / 1

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40418

Product Number

1

Dosage Form

-

Strength

500MG/15ML;7.5MG/15ML

Approval Date

2001-06-27

Regulatory Status

Discontinued

2003
29 Aug
Discontinued Application: 40508

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

500MG/15ML;10MG/15ML

Approval Date

2003-08-29

40508 / 1

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

40508

Product Number

1

Dosage Form

-

Strength

500MG/15ML;10MG/15ML

Approval Date

2003-08-29

Regulatory Status

Discontinued

1985
19 Jul
Discontinued Application: 88956

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

1985-07-19

88956 / 1

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

88956

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

1985-07-19

Regulatory Status

Discontinued

1985
09 Aug
Discontinued Application: 89006

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

1985-08-09

89006 / 1

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

89006

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

1985-08-09

Regulatory Status

Discontinued

1984
22 May
Discontinued Application: 87846

Drug Name

IMIPRAMINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

1984-05-22

87846 / 2

Active Ingredient

IMIPRAMINE HYDROCHLORIDE

Application Number

87846

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

1984-05-22

Regulatory Status

Discontinued

1984
22 May
Discontinued Application: 87846

Drug Name

IMIPRAMINE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

25MG

Approval Date

1984-05-22

87846 / 3

Active Ingredient

IMIPRAMINE HYDROCHLORIDE

Application Number

87846

Product Number

3

Dosage Form

-

Strength

25MG

Approval Date

1984-05-22

Regulatory Status

Discontinued

1982
08 Jul
Discontinued Application: 87336

Drug Name

LORCET-HD

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

1982-07-08

87336 / 1

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

87336

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

1982-07-08

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 87075

Drug Name

MD-50

Product Number

1

Dosage Form

-

Strength

50%

Approval Date

1982-01-01

87075 / 1

Active Ingredient

DIATRIZOATE SODIUM

Application Number

87075

Product Number

1

Dosage Form

-

Strength

50%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 87074

Drug Name

MD-60

Product Number

1

Dosage Form

-

Strength

52%;8%

Approval Date

1982-01-01

87074 / 1

Active Ingredient

DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

Application Number

87074

Product Number

1

Dosage Form

-

Strength

52%;8%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 87073

Drug Name

MD-76

Product Number

1

Dosage Form

-

Strength

66%;10%

Approval Date

1982-01-01

87073 / 1

Active Ingredient

DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

Application Number

87073

Product Number

1

Dosage Form

-

Strength

66%;10%

Approval Date

1982-01-01

Regulatory Status

Discontinued

2000
13 Jun
Discontinued Application: 40352

Drug Name

MEPERIDINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

2000-06-13

40352 / 1

Active Ingredient

MEPERIDINE HYDROCHLORIDE

Application Number

40352

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

2000-06-13

Regulatory Status

Discontinued

2000
13 Jun
Discontinued Application: 40352

Drug Name

MEPERIDINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

2000-06-13

40352 / 2

Active Ingredient

MEPERIDINE HYDROCHLORIDE

Application Number

40352

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

2000-06-13

Regulatory Status

Discontinued

1997
12 May
Discontinued Application: 40163

Drug Name

MEPERIDINE HYDROCHLORIDE PRESERVATIVE FREE

Product Number

1

Dosage Form

-

Strength

10MG/ML

Approval Date

1997-05-12

40163 / 1

Active Ingredient

MEPERIDINE HYDROCHLORIDE

Application Number

40163

Product Number

1

Dosage Form

-

Strength

10MG/ML

Approval Date

1997-05-12

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 6383

Drug Name

METHADONE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

50GM/BOT

Approval Date

1982-01-01

6383 / 2

Active Ingredient

METHADONE HYDROCHLORIDE

Application Number

6383

Product Number

2

Dosage Form

-

Strength

50GM/BOT

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 6383

Drug Name

METHADONE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

100GM/BOT

Approval Date

1982-01-01

6383 / 3

Active Ingredient

METHADONE HYDROCHLORIDE

Application Number

6383

Product Number

3

Dosage Form

-

Strength

100GM/BOT

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 6383

Drug Name

METHADONE HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

500GM/BOT

Approval Date

1982-01-01

6383 / 4

Active Ingredient

METHADONE HYDROCHLORIDE

Application Number

6383

Product Number

4

Dosage Form

-

Strength

500GM/BOT

Approval Date

1982-01-01

Regulatory Status

Discontinued

1993
15 Apr
Discontinued Application: 40050

Drug Name

METHADOSE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1993-04-15

40050 / 1

Active Ingredient

METHADONE HYDROCHLORIDE

Application Number

40050

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1993-04-15

Regulatory Status

Discontinued

1993
15 Apr
Discontinued Application: 40050

Drug Name

METHADOSE

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

1993-04-15

40050 / 2

Active Ingredient

METHADONE HYDROCHLORIDE

Application Number

40050

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

1993-04-15

Regulatory Status

Discontinued

2003
15 Apr
Discontinued Application: 21475

Drug Name

METHYLIN

Product Number

1

Dosage Form

-

Strength

2.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2003-04-15

21475 / 1

Active Ingredient

METHYLPHENIDATE HYDROCHLORIDE

Application Number

21475

Product Number

1

Dosage Form

-

Strength

2.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2003-04-15

Regulatory Status

Discontinued

2003
15 Apr
Discontinued Application: 21475

Drug Name

METHYLIN

Product Number

2

Dosage Form

-

Strength

5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2003-04-15

21475 / 2

Active Ingredient

METHYLPHENIDATE HYDROCHLORIDE

Application Number

21475

Product Number

2

Dosage Form

-

Strength

5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2003-04-15

Regulatory Status

Discontinued

2003
15 Apr
Discontinued Application: 21475

Drug Name

METHYLIN

Product Number

3

Dosage Form

-

Strength

10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2003-04-15

21475 / 3

Active Ingredient

METHYLPHENIDATE HYDROCHLORIDE

Application Number

21475

Product Number

3

Dosage Form

-

Strength

10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2003-04-15

Regulatory Status

Discontinued

2012
28 Dec
Discontinued Application: 202608

Drug Name

METHYLPHENIDATE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

27MG

Approval Date

2012-12-28

202608 / 1

Active Ingredient

METHYLPHENIDATE HYDROCHLORIDE

Application Number

202608

Product Number

1

Dosage Form

-

Strength

27MG

Approval Date

2012-12-28

Regulatory Status

Discontinued

2012
28 Dec
Discontinued Application: 202608

Drug Name

METHYLPHENIDATE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

36MG

Approval Date

2012-12-28

202608 / 2

Active Ingredient

METHYLPHENIDATE HYDROCHLORIDE

Application Number

202608

Product Number

2

Dosage Form

-

Strength

36MG

Approval Date

2012-12-28

Regulatory Status

Discontinued

2012
28 Dec
Discontinued Application: 202608

Drug Name

METHYLPHENIDATE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

54MG

Approval Date

2012-12-28

202608 / 3

Active Ingredient

METHYLPHENIDATE HYDROCHLORIDE

Application Number

202608

Product Number

3

Dosage Form

-

Strength

54MG

Approval Date

2012-12-28

Regulatory Status

Discontinued

1996
03 Jul
Discontinued Application: 20631

Drug Name

MORPHINE SULFATE

Product Number

1

Dosage Form

-

Strength

1MG/ML

Approval Date

1996-07-03

20631 / 1

Active Ingredient

MORPHINE SULFATE

Application Number

20631

Product Number

1

Dosage Form

-

Strength

1MG/ML

Approval Date

1996-07-03

Regulatory Status

Discontinued

1996
03 Jul
Discontinued Application: 20631

Drug Name

MORPHINE SULFATE

Product Number

2

Dosage Form

-

Strength

2MG/ML

Approval Date

1996-07-03

20631 / 2

Active Ingredient

MORPHINE SULFATE

Application Number

20631

Product Number

2

Dosage Form

-

Strength

2MG/ML

Approval Date

1996-07-03

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17454

Drug Name

OSTEOSCAN

Product Number

1

Dosage Form

-

Strength

N/A

Approval Date

1982-01-01

17454 / 1

Active Ingredient

TECHNETIUM TC-99M ETIDRONATE KIT

Application Number

17454

Product Number

1

Dosage Form

-

Strength

N/A

Approval Date

1982-01-01

Regulatory Status

Discontinued

1998
04 Aug
Discontinued Application: 40257

Drug Name

OXYCODONE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

1998-08-04

40257 / 1

Active Ingredient

ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE

Application Number

40257

Product Number

1

Dosage Form

-

Strength

500MG;5MG

Approval Date

1998-08-04

Regulatory Status

Discontinued

2004
30 Jun
Discontinued Application: 40550

Drug Name

OXYCODONE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

500MG;7.5MG

Approval Date

2004-06-30

40550 / 1

Active Ingredient

ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE

Application Number

40550

Product Number

1

Dosage Form

-

Strength

500MG;7.5MG

Approval Date

2004-06-30

Regulatory Status

Discontinued

2004
30 Jun
Discontinued Application: 40550

Drug Name

OXYCODONE AND ACETAMINOPHEN

Product Number

2

Dosage Form

-

Strength

650MG;10MG

Approval Date

2004-06-30

40550 / 2

Active Ingredient

ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE

Application Number

40550

Product Number

2

Dosage Form

-

Strength

650MG;10MG

Approval Date

2004-06-30

Regulatory Status

Discontinued

2006
29 Sep
Discontinued Application: 40680

Drug Name

OXYCODONE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

325MG/5ML;5MG/5ML

Approval Date

2006-09-29

40680 / 1

Active Ingredient

ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE

Application Number

40680

Product Number

1

Dosage Form

-

Strength

325MG/5ML;5MG/5ML

Approval Date

2006-09-29

Regulatory Status

Discontinued

2013
25 Apr
Discontinued Application: 202321

Drug Name

OXYMORPHONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2013-04-25

202321 / 1

Active Ingredient

OXYMORPHONE HYDROCHLORIDE

Application Number

202321

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2013-04-25

Regulatory Status

Discontinued

2013
25 Apr
Discontinued Application: 202321

Drug Name

OXYMORPHONE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2013-04-25

202321 / 2

Active Ingredient

OXYMORPHONE HYDROCHLORIDE

Application Number

202321

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2013-04-25

Regulatory Status

Discontinued

2014
27 Jun
Discontinued Application: 202946

Drug Name

OXYMORPHONE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2014-06-27

202946 / 1

Active Ingredient

OXYMORPHONE HYDROCHLORIDE

Application Number

202946

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2014-06-27

Regulatory Status

Discontinued

2014
27 Jun
Discontinued Application: 202946

Drug Name

OXYMORPHONE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

7.5MG

Approval Date

2014-06-27

202946 / 2

Active Ingredient

OXYMORPHONE HYDROCHLORIDE

Application Number

202946

Product Number

2

Dosage Form

-

Strength

7.5MG

Approval Date

2014-06-27

Regulatory Status

Discontinued

2014
27 Jun
Discontinued Application: 202946

Drug Name

OXYMORPHONE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

2014-06-27

202946 / 3

Active Ingredient

OXYMORPHONE HYDROCHLORIDE

Application Number

202946

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

2014-06-27

Regulatory Status

Discontinued

2014
27 Jun
Discontinued Application: 202946

Drug Name

OXYMORPHONE HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

15MG

Approval Date

2014-06-27

202946 / 4

Active Ingredient

OXYMORPHONE HYDROCHLORIDE

Application Number

202946

Product Number

4

Dosage Form

-

Strength

15MG

Approval Date

2014-06-27

Regulatory Status

Discontinued

2014
27 Jun
Discontinued Application: 202946

Drug Name

OXYMORPHONE HYDROCHLORIDE

Product Number

5

Dosage Form

-

Strength

20MG

Approval Date

2014-06-27

202946 / 5

Active Ingredient

OXYMORPHONE HYDROCHLORIDE

Application Number

202946

Product Number

5

Dosage Form

-

Strength

20MG

Approval Date

2014-06-27

Regulatory Status

Discontinued

2014
27 Jun
Discontinued Application: 202946

Drug Name

OXYMORPHONE HYDROCHLORIDE

Product Number

6

Dosage Form

-

Strength

30MG

Approval Date

2014-06-27

202946 / 6

Active Ingredient

OXYMORPHONE HYDROCHLORIDE

Application Number

202946

Product Number

6

Dosage Form

-

Strength

30MG

Approval Date

2014-06-27

Regulatory Status

Discontinued

2014
27 Jun
Discontinued Application: 202946

Drug Name

OXYMORPHONE HYDROCHLORIDE

Product Number

7

Dosage Form

-

Strength

40MG

Approval Date

2014-06-27

202946 / 7

Active Ingredient

OXYMORPHONE HYDROCHLORIDE

Application Number

202946

Product Number

7

Dosage Form

-

Strength

40MG

Approval Date

2014-06-27

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 18012

Drug Name

PAMELOR

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE/5ML

Approval Date

1982-01-01

18012 / 1

Active Ingredient

NORTRIPTYLINE HYDROCHLORIDE

Application Number

18012

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 18013

Drug Name

PAMELOR

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

1982-01-01

18013 / 1

Active Ingredient

NORTRIPTYLINE HYDROCHLORIDE

Application Number

18013

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 18013

Drug Name

PAMELOR

Product Number

2

Dosage Form

-

Strength

EQ 25MG BASE

Approval Date

1982-01-01

18013 / 2

Active Ingredient

NORTRIPTYLINE HYDROCHLORIDE

Application Number

18013

Product Number

2

Dosage Form

-

Strength

EQ 25MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 18013

Drug Name

PAMELOR

Product Number

3

Dosage Form

-

Strength

EQ 75MG BASE

Approval Date

1982-01-01

18013 / 3

Active Ingredient

NORTRIPTYLINE HYDROCHLORIDE

Application Number

18013

Product Number

3

Dosage Form

-

Strength

EQ 75MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 18013

Drug Name

PAMELOR

Product Number

4

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

1982-01-01

18013 / 4

Active Ingredient

NORTRIPTYLINE HYDROCHLORIDE

Application Number

18013

Product Number

4

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

2001
30 Mar
Discontinued Application: 75726

Drug Name

PEMOLINE

Product Number

1

Dosage Form

-

Strength

75MG

Approval Date

2001-03-30

75726 / 1

Active Ingredient

PEMOLINE

Application Number

75726

Product Number

1

Dosage Form

-

Strength

75MG

Approval Date

2001-03-30

Regulatory Status

Discontinued

2001
30 Mar
Discontinued Application: 75726

Drug Name

PEMOLINE

Product Number

2

Dosage Form

-

Strength

37.5MG

Approval Date

2001-03-30

75726 / 2

Active Ingredient

PEMOLINE

Application Number

75726

Product Number

2

Dosage Form

-

Strength

37.5MG

Approval Date

2001-03-30

Regulatory Status

Discontinued

2001
30 Mar
Discontinued Application: 75726

Drug Name

PEMOLINE

Product Number

3

Dosage Form

-

Strength

18.75MG

Approval Date

2001-03-30

75726 / 3

Active Ingredient

PEMOLINE

Application Number

75726

Product Number

3

Dosage Form

-

Strength

18.75MG

Approval Date

2001-03-30

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17551

Drug Name

PERCHLORACAP

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

17551 / 1

Active Ingredient

POTASSIUM PERCHLORATE

Application Number

17551

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
26 May
Discontinued Application: 87214

Drug Name

PHENDIMETRAZINE TARTRATE

Product Number

1

Dosage Form

-

Strength

105MG

Approval Date

1982-05-26

87214 / 1

Active Ingredient

PHENDIMETRAZINE TARTRATE

Application Number

87214

Product Number

1

Dosage Form

-

Strength

105MG

Approval Date

1982-05-26

Regulatory Status

Discontinued

1982
16 Aug
Discontinued Application: 88020

Drug Name

PHENDIMETRAZINE TARTRATE

Product Number

1

Dosage Form

-

Strength

105MG

Approval Date

1982-08-16

88020 / 1

Active Ingredient

PHENDIMETRAZINE TARTRATE

Application Number

88020

Product Number

1

Dosage Form

-

Strength

105MG

Approval Date

1982-08-16

Regulatory Status

Discontinued

1982
16 Aug
Discontinued Application: 88028

Drug Name

PHENDIMETRAZINE TARTRATE

Product Number

1

Dosage Form

-

Strength

105MG

Approval Date

1982-08-16

88028 / 1

Active Ingredient

PHENDIMETRAZINE TARTRATE

Application Number

88028

Product Number

1

Dosage Form

-

Strength

105MG

Approval Date

1982-08-16

Regulatory Status

Discontinued

1982
13 Sep
Discontinued Application: 88062

Drug Name

PHENDIMETRAZINE TARTRATE

Product Number

1

Dosage Form

-

Strength

105MG

Approval Date

1982-09-13

88062 / 1

Active Ingredient

PHENDIMETRAZINE TARTRATE

Application Number

88062

Product Number

1

Dosage Form

-

Strength

105MG

Approval Date

1982-09-13

Regulatory Status

Discontinued

1982
10 Sep
Discontinued Application: 88063

Drug Name

PHENDIMETRAZINE TARTRATE

Product Number

1

Dosage Form

-

Strength

105MG

Approval Date

1982-09-10

88063 / 1

Active Ingredient

PHENDIMETRAZINE TARTRATE

Application Number

88063

Product Number

1

Dosage Form

-

Strength

105MG

Approval Date

1982-09-10

Regulatory Status

Discontinued

1982
18 Oct
Discontinued Application: 88111

Drug Name

PHENDIMETRAZINE TARTRATE

Product Number

1

Dosage Form

-

Strength

105MG

Approval Date

1982-10-18

88111 / 1

Active Ingredient

PHENDIMETRAZINE TARTRATE

Application Number

88111

Product Number

1

Dosage Form

-

Strength

105MG

Approval Date

1982-10-18

Regulatory Status

Discontinued

2001
02 Feb
Discontinued Application: 75738

Drug Name

PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

650MG;100MG

Approval Date

2001-02-02

75738 / 1

Active Ingredient

ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE

Application Number

75738

Product Number

1

Dosage Form

-

Strength

650MG;100MG

Approval Date

2001-02-02

Regulatory Status

Discontinued

1985
18 Mar
Discontinued Application: 18843

Drug Name

PSEUDOEPHEDRINE HYDROCHLORIDE AND CHLORPHENIRAMINE MALEATE

Product Number

1

Dosage Form

-

Strength

12MG;120MG

Approval Date

1985-03-18

18843 / 1

Active Ingredient

CHLORPHENIRAMINE MALEATE; PSEUDOEPHEDRINE HYDROCHLORIDE

Application Number

18843

Product Number

1

Dosage Form

-

Strength

12MG;120MG

Approval Date

1985-03-18

Regulatory Status

Discontinued

1985
20 Mar
Discontinued Application: 18844

Drug Name

PSEUDOEPHEDRINE HYDROCHLORIDE AND CHLORPHENIRAMINE MALEATE

Product Number

1

Dosage Form

-

Strength

8MG;120MG

Approval Date

1985-03-20

18844 / 1

Active Ingredient

CHLORPHENIRAMINE MALEATE; PSEUDOEPHEDRINE HYDROCHLORIDE

Application Number

18844

Product Number

1

Dosage Form

-

Strength

8MG;120MG

Approval Date

1985-03-20

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17098

Drug Name

SELENOMETHIONINE SE 75

Product Number

1

Dosage Form

-

Strength

100uCi/ML

Approval Date

1982-01-01

17098 / 1

Active Ingredient

SELENOMETHIONINE SE-75

Application Number

17098

Product Number

1

Dosage Form

-

Strength

100uCi/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17725

Drug Name

SODIUM PERTECHNETATE TC 99M

Product Number

1

Dosage Form

-

Strength

10-60mCi/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

17725 / 1

Active Ingredient

TECHNETIUM TC-99M SODIUM PERTECHNETATE

Application Number

17725

Product Number

1

Dosage Form

-

Strength

10-60mCi/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: 11777

Drug Name

SODIUM PHOSPHATE P 32

Product Number

1

Dosage Form

-

Strength

0.67mCi/ML

Approval Date

1982-01-01

11777 / 1

Active Ingredient

SODIUM PHOSPHATE P-32

Application Number

11777

Product Number

1

Dosage Form

-

Strength

0.67mCi/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 11777

Drug Name

SODIUM PHOSPHATE P 32

Product Number

2

Dosage Form

-

Strength

1.5mCi/VIAL

Approval Date

1982-01-01

11777 / 2

Active Ingredient

SODIUM PHOSPHATE P-32

Application Number

11777

Product Number

2

Dosage Form

-

Strength

1.5mCi/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 87193

Drug Name

SOMOPHYLLIN-CRT

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

87193 / 1

Active Ingredient

THEOPHYLLINE

Application Number

87193

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 87194

Drug Name

SOMOPHYLLIN-CRT

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

87194 / 1

Active Ingredient

THEOPHYLLINE

Application Number

87194

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1985
27 Feb
Discontinued Application: 87763

Drug Name

SOMOPHYLLIN-CRT

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1985-02-27

87763 / 1

Active Ingredient

THEOPHYLLINE

Application Number

87763

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1985-02-27

Regulatory Status

Discontinued

1985
27 Feb
Discontinued Application: 88382

Drug Name

SOMOPHYLLIN-CRT

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1985-02-27

88382 / 1

Active Ingredient

THEOPHYLLINE

Application Number

88382

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1985-02-27

Regulatory Status

Discontinued

1985
27 Feb
Discontinued Application: 88383

Drug Name

SOMOPHYLLIN-CRT

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

1985-02-27

88383 / 1

Active Ingredient

THEOPHYLLINE

Application Number

88383

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

1985-02-27

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17059

Drug Name

TECHNECOLL

Product Number

1

Dosage Form

-

Strength

N/A

Approval Date

1982-01-01

17059 / 1

Active Ingredient

TECHNETIUM TC-99M SULFUR COLLOID KIT

Application Number

17059

Product Number

1

Dosage Form

-

Strength

N/A

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17724

Drug Name

TECHNETIUM TC 99M SULFUR COLLOID

Product Number

1

Dosage Form

-

Strength

3mCi/ML

Approval Date

1982-01-01

17724 / 1

Active Ingredient

TECHNETIUM TC-99M SULFUR COLLOID

Application Number

17724

Product Number

1

Dosage Form

-

Strength

3mCi/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1990
15 May
Discontinued Application: 89405

Drug Name

TENCON

Product Number

1

Dosage Form

-

Strength

650MG;50MG

Approval Date

1990-05-15

89405 / 1

Active Ingredient

ACETAMINOPHEN; BUTALBITAL

Application Number

89405

Product Number

1

Dosage Form

-

Strength

650MG;50MG

Approval Date

1990-05-15

Regulatory Status

Discontinued

1984
22 May
Discontinued Application: 87846

Drug Name

TOFRANIL

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1984-05-22

87846 / 1

Active Ingredient

IMIPRAMINE HYDROCHLORIDE

Application Number

87846

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1984-05-22

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17090

Drug Name

TOFRANIL-PM

Product Number

1

Dosage Form

-

Strength

EQ 75MG HYDROCHLORIDE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

17090 / 1

Active Ingredient

IMIPRAMINE PAMOATE

Application Number

17090

Product Number

1

Dosage Form

-

Strength

EQ 75MG HYDROCHLORIDE **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: 17090

Drug Name

TOFRANIL-PM

Product Number

2

Dosage Form

-

Strength

EQ 150MG HYDROCHLORIDE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

17090 / 2

Active Ingredient

IMIPRAMINE PAMOATE

Application Number

17090

Product Number

2

Dosage Form

-

Strength

EQ 150MG HYDROCHLORIDE **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: 17090

Drug Name

TOFRANIL-PM

Product Number

3

Dosage Form

-

Strength

EQ 125MG HYDROCHLORIDE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

17090 / 3

Active Ingredient

IMIPRAMINE PAMOATE

Application Number

17090

Product Number

3

Dosage Form

-

Strength

EQ 125MG HYDROCHLORIDE **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: 17090

Drug Name

TOFRANIL-PM

Product Number

4

Dosage Form

-

Strength

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

Approval Date

1982-01-01

17090 / 4

Active Ingredient

IMIPRAMINE PAMOATE

Application Number

17090

Product Number

4

Dosage Form

-

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

2002
25 Jun
Discontinued Application: 75983

Drug Name

TRAMADOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

2002-06-25

75983 / 1

Active Ingredient

TRAMADOL HYDROCHLORIDE

Application Number

75983

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

2002-06-25

Regulatory Status

Discontinued

1985
19 Jun
Discontinued Application: 89023

Drug Name

TRIAD

Product Number

1

Dosage Form

-

Strength

325MG;50MG;40MG

Approval Date

1985-06-19

89023 / 1

Active Ingredient

ACETAMINOPHEN; BUTALBITAL; CAFFEINE

Application Number

89023

Product Number

1

Dosage Form

-

Strength

325MG;50MG;40MG

Approval Date

1985-06-19

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 16783

Drug Name

VASCORAY

Product Number

1

Dosage Form

-

Strength

52%;26%

Approval Date

1982-01-01

16783 / 1

Active Ingredient

IOTHALAMATE MEGLUMINE; IOTHALAMATE SODIUM

Application Number

16783

Product Number

1

Dosage Form

-

Strength

52%;26%

Approval Date

1982-01-01

Regulatory Status

Discontinued

2021
28 Jul
Discontinued Application: 212626

Drug Name

VIGABATRIN

Product Number

1

Dosage Form

-

Strength

500MG/PACKET

Approval Date

2021-07-28

212626 / 1

Active Ingredient

VIGABATRIN

Application Number

212626

Product Number

1

Dosage Form

-

Strength

500MG/PACKET

Approval Date

2021-07-28

Regulatory Status

Discontinued

2014
11 Mar
Discontinued Application: 204031

Drug Name

XARTEMIS XR

Product Number

1

Dosage Form

-

Strength

325MG;7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2014-03-11

204031 / 1

Active Ingredient

ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE

Application Number

204031

Product Number

1

Dosage Form

-

Strength

325MG;7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2014-03-11

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17262

Drug Name

XENEISOL

Product Number

2

Dosage Form

-

Strength

18-25mCi/AMP

Approval Date

1982-01-01

17262 / 2

Active Ingredient

XENON XE-133

Application Number

17262

Product Number

2

Dosage Form

-

Strength

18-25mCi/AMP

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Oct
Discontinued Application: 18536

Drug Name

XENON XE 127

Product Number

1

Dosage Form

-

Strength

5mCi/VIAL

Approval Date

1982-10-01

18536 / 1

Active Ingredient

XENON XE-127

Application Number

18536

Product Number

1

Dosage Form

-

Strength

5mCi/VIAL

Approval Date

1982-10-01

Regulatory Status

Discontinued

1982
01 Oct
Discontinued Application: 18536

Drug Name

XENON XE 127

Product Number

2

Dosage Form

-

Strength

10mCi/VIAL

Approval Date

1982-10-01

18536 / 2

Active Ingredient

XENON XE-127

Application Number

18536

Product Number

2

Dosage Form

-

Strength

10mCi/VIAL

Approval Date

1982-10-01

Regulatory Status

Discontinued

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Drug Status Breakdown
121 total
  • 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

ANEXSIA

Application Number

40468

Product Number

1

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Dosage Form

-

Strength

750MG;10MG

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

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