Perrigo Company plc Discontinued
FDA Approved Drugs

Perrigo Company plc 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 48
  • Latest Approval Date Dec 22, 2011
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
80
View
Unclassified
1
View
Discontinued
48
View
OTC
31
View
Company Overview

Company

Perrigo Company plc Discontinued

Country

Ireland

Website

Visit Website

Email

enquiries@pharmacompass.com

Social Profiles

LinkedIn X / Twitter
Company Snapshot

Perrigo Company plc Discontinued

The Sharp Building Hogan Place Dublin 2

Ireland

www.perrigo.com/ enquiries@pharmacompass.com View on Map
FDA Approved Drug Records ( 48 records )
1987
10 Apr
Discontinued Application: 71292

Drug Name

ANTITUSSIVE

Product Number

1

Dosage Form

-

Strength

12.5MG/5ML

Approval Date

1987-04-10

71292 / 1

Active Ingredient

DIPHENHYDRAMINE HYDROCHLORIDE

Application Number

71292

Product Number

1

Dosage Form

-

Strength

12.5MG/5ML

Approval Date

1987-04-10

Regulatory Status

Discontinued

1990
31 Jan
Discontinued Application: 72526

Drug Name

BETAMETHASONE DIPROPIONATE

Product Number

1

Dosage Form

-

Strength

EQ 0.05% BASE

Approval Date

1990-01-31

72526 / 1

Active Ingredient

BETAMETHASONE DIPROPIONATE

Application Number

72526

Product Number

1

Dosage Form

-

Strength

EQ 0.05% BASE

Approval Date

1990-01-31

Regulatory Status

Discontinued

1990
31 Jan
Discontinued Application: 72536

Drug Name

BETAMETHASONE DIPROPIONATE

Product Number

1

Dosage Form

-

Strength

EQ 0.05% BASE

Approval Date

1990-01-31

72536 / 1

Active Ingredient

BETAMETHASONE DIPROPIONATE

Application Number

72536

Product Number

1

Dosage Form

-

Strength

EQ 0.05% BASE

Approval Date

1990-01-31

Regulatory Status

Discontinued

1997
26 Nov
Discontinued Application: 74579

Drug Name

BETAMETHASONE DIPROPIONATE

Product Number

1

Dosage Form

-

Strength

EQ 0.05% BASE

Approval Date

1997-11-26

74579 / 1

Active Ingredient

BETAMETHASONE DIPROPIONATE

Application Number

74579

Product Number

1

Dosage Form

-

Strength

EQ 0.05% BASE

Approval Date

1997-11-26

Regulatory Status

Discontinued

1986
10 Jun
Discontinued Application: 70053

Drug Name

BETAMETHASONE VALERATE

Product Number

1

Dosage Form

-

Strength

EQ 0.1% BASE

Approval Date

1986-06-10

70053 / 1

Active Ingredient

BETAMETHASONE VALERATE

Application Number

70053

Product Number

1

Dosage Form

-

Strength

EQ 0.1% BASE

Approval Date

1986-06-10

Regulatory Status

Discontinued

1987
23 Dec
Discontinued Application: 71478

Drug Name

BETAMETHASONE VALERATE

Product Number

1

Dosage Form

-

Strength

EQ 0.1% BASE

Approval Date

1987-12-23

71478 / 1

Active Ingredient

BETAMETHASONE VALERATE

Application Number

71478

Product Number

1

Dosage Form

-

Strength

EQ 0.1% BASE

Approval Date

1987-12-23

Regulatory Status

Discontinued

1987
08 Dec
Discontinued Application: 72097

Drug Name

CAP-PROFEN

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1987-12-08

72097 / 1

Active Ingredient

IBUPROFEN

Application Number

72097

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1987-12-08

Regulatory Status

Discontinued

1998
19 Jun
Discontinued Application: 74972

Drug Name

CIMETIDINE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1998-06-19

74972 / 1

Active Ingredient

CIMETIDINE

Application Number

74972

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1998-06-19

Regulatory Status

Discontinued

2001
12 Dec
Discontinued Application: 75427

Drug Name

CROMOLYN SODIUM

Product Number

1

Dosage Form

-

Strength

5.2MG/SPRAY

Approval Date

2001-12-12

75427 / 1

Active Ingredient

CROMOLYN SODIUM

Application Number

75427

Product Number

1

Dosage Form

-

Strength

5.2MG/SPRAY

Approval Date

2001-12-12

Regulatory Status

Discontinued

2011
22 Dec
Discontinued Application: 78361

Drug Name

DESLORATADINE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2011-12-22

78361 / 1

Active Ingredient

DESLORATADINE

Application Number

78361

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2011-12-22

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83061

Drug Name

DIPHENHYDRAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

83061 / 1

Active Ingredient

DIPHENHYDRAMINE HYDROCHLORIDE

Application Number

83061

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83061

Drug Name

DIPHENHYDRAMINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

83061 / 2

Active Ingredient

DIPHENHYDRAMINE HYDROCHLORIDE

Application Number

83061

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83063

Drug Name

DIPHENHYDRAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

12.5MG/5ML

Approval Date

1982-01-01

83063 / 1

Active Ingredient

DIPHENHYDRAMINE HYDROCHLORIDE

Application Number

83063

Product Number

1

Dosage Form

-

Strength

12.5MG/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

2003
22 Aug
Discontinued Application: 75715

Drug Name

FAMOTIDINE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2003-08-22

75715 / 1

Active Ingredient

FAMOTIDINE

Application Number

75715

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2003-08-22

Regulatory Status

Discontinued

1982
04 Mar
Discontinued Application: 86810

Drug Name

FLUOCINOLONE ACETONIDE

Product Number

1

Dosage Form

-

Strength

0.01%

Approval Date

1982-03-04

86810 / 1

Active Ingredient

FLUOCINOLONE ACETONIDE

Application Number

86810

Product Number

1

Dosage Form

-

Strength

0.01%

Approval Date

1982-03-04

Regulatory Status

Discontinued

1982
04 Mar
Discontinued Application: 86811

Drug Name

FLUOCINOLONE ACETONIDE

Product Number

1

Dosage Form

-

Strength

0.025%

Approval Date

1982-03-04

86811 / 1

Active Ingredient

FLUOCINOLONE ACETONIDE

Application Number

86811

Product Number

1

Dosage Form

-

Strength

0.025%

Approval Date

1982-03-04

Regulatory Status

Discontinued

1988
13 Jul
Discontinued Application: 71790

Drug Name

FLUOCINONIDE

Product Number

1

Dosage Form

-

Strength

0.05%

Approval Date

1988-07-13

71790 / 1

Active Ingredient

FLUOCINONIDE

Application Number

71790

Product Number

1

Dosage Form

-

Strength

0.05%

Approval Date

1988-07-13

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84969

Drug Name

HYDROCORTISONE

Product Number

3

Dosage Form

-

Strength

0.5%

Approval Date

1982-01-01

84969 / 3

Active Ingredient

HYDROCORTISONE

Application Number

84969

Product Number

3

Dosage Form

-

Strength

0.5%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84970

Drug Name

HYDROCORTISONE

Product Number

2

Dosage Form

-

Strength

0.5%

Approval Date

1982-01-01

84970 / 2

Active Ingredient

HYDROCORTISONE

Application Number

84970

Product Number

2

Dosage Form

-

Strength

0.5%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85026

Drug Name

HYDROCORTISONE

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

85026 / 1

Active Ingredient

HYDROCORTISONE

Application Number

85026

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85028

Drug Name

HYDROCORTISONE

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

85028 / 1

Active Ingredient

HYDROCORTISONE

Application Number

85028

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85662

Drug Name

HYDROCORTISONE

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

1982-01-01

85662 / 1

Active Ingredient

HYDROCORTISONE

Application Number

85662

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85663

Drug Name

HYDROCORTISONE

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

85663 / 1

Active Ingredient

HYDROCORTISONE

Application Number

85663

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1987
08 Dec
Discontinued Application: 72098

Drug Name

IBUPROFEN

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1987-12-08

72098 / 1

Active Ingredient

IBUPROFEN

Application Number

72098

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1987-12-08

Regulatory Status

Discontinued

2002
14 Mar
Discontinued Application: 75995

Drug Name

IBUPROFEN

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

2002-03-14

75995 / 1

Active Ingredient

IBUPROFEN

Application Number

75995

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

2002-03-14

Regulatory Status

Discontinued

2004
16 Jan
Discontinued Application: 76359

Drug Name

IBUPROFEN

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

2004-01-16

76359 / 1

Active Ingredient

IBUPROFEN

Application Number

76359

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

2004-01-16

Regulatory Status

Discontinued

2003
05 Nov
Discontinued Application: 76478

Drug Name

IBUPROFEN AND PSEUDOEPHEDRINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

100MG/5ML;15MG/5ML

Approval Date

2003-11-05

76478 / 1

Active Ingredient

IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE

Application Number

76478

Product Number

1

Dosage Form

-

Strength

100MG/5ML;15MG/5ML

Approval Date

2003-11-05

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83060

Drug Name

ISONIAZID

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

83060 / 1

Active Ingredient

ISONIAZID

Application Number

83060

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

2002
07 Feb
Discontinued Application: 75364

Drug Name

KETOPROFEN

Product Number

1

Dosage Form

-

Strength

12.5MG

Approval Date

2002-02-07

75364 / 1

Active Ingredient

KETOPROFEN

Application Number

75364

Product Number

1

Dosage Form

-

Strength

12.5MG

Approval Date

2002-02-07

Regulatory Status

Discontinued

1992
21 Jan
Discontinued Application: 73243

Drug Name

LOPERAMIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

1MG/5ML

Approval Date

1992-01-21

73243 / 1

Active Ingredient

LOPERAMIDE HYDROCHLORIDE

Application Number

73243

Product Number

1

Dosage Form

-

Strength

1MG/5ML

Approval Date

1992-01-21

Regulatory Status

Discontinued

1992
30 Oct
Discontinued Application: 74194

Drug Name

LOPERAMIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1992-10-30

74194 / 1

Active Ingredient

LOPERAMIDE HYDROCHLORIDE

Application Number

74194

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1992-10-30

Regulatory Status

Discontinued

2002
30 Aug
Discontinued Application: 76029

Drug Name

LOPERAMIDE HYDROCHLORIDE AND SIMETHICONE

Product Number

1

Dosage Form

-

Strength

2MG;125MG

Approval Date

2002-08-30

76029 / 1

Active Ingredient

LOPERAMIDE HYDROCHLORIDE; SIMETHICONE

Application Number

76029

Product Number

1

Dosage Form

-

Strength

2MG;125MG

Approval Date

2002-08-30

Regulatory Status

Discontinued

2004
24 Jun
Discontinued Application: 21512

Drug Name

LORATADINE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2004-06-24

21512 / 1

Active Ingredient

LORATADINE

Application Number

21512

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2004-06-24

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84546

Drug Name

MEPROBAMATE

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

84546 / 1

Active Ingredient

MEPROBAMATE

Application Number

84546

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84547

Drug Name

MEPROBAMATE

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

1982-01-01

84547 / 1

Active Ingredient

MEPROBAMATE

Application Number

84547

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1997
20 Mar
Discontinued Application: 74395

Drug Name

MICONAZOLE NITRATE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1997-03-20

74395 / 1

Active Ingredient

MICONAZOLE NITRATE

Application Number

74395

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1997-03-20

Regulatory Status

Discontinued

2002
15 Mar
Discontinued Application: 75737

Drug Name

MINOXIDIL EXTRA STRENGTH (FOR MEN)

Product Number

1

Dosage Form

-

Strength

5%

Approval Date

2002-03-15

75737 / 1

Active Ingredient

MINOXIDIL

Application Number

75737

Product Number

1

Dosage Form

-

Strength

5%

Approval Date

2002-03-15

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84968

Drug Name

NITROFURAZONE

Product Number

1

Dosage Form

-

Strength

0.2%

Approval Date

1982-01-01

84968 / 1

Active Ingredient

NITROFURAZONE

Application Number

84968

Product Number

1

Dosage Form

-

Strength

0.2%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85130

Drug Name

NITROFURAZONE

Product Number

1

Dosage Form

-

Strength

0.2%

Approval Date

1982-01-01

85130 / 1

Active Ingredient

NITROFURAZONE

Application Number

85130

Product Number

1

Dosage Form

-

Strength

0.2%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1985
06 Jun
Discontinued Application: 62186

Drug Name

NYSTATIN AND TRIAMCINOLONE ACETONIDE

Product Number

2

Dosage Form

-

Strength

100,000 UNITS/GM;0.1%

Approval Date

1985-06-06

62186 / 2

Active Ingredient

NYSTATIN; TRIAMCINOLONE ACETONIDE

Application Number

62186

Product Number

2

Dosage Form

-

Strength

100,000 UNITS/GM;0.1%

Approval Date

1985-06-06

Regulatory Status

Discontinued

1985
10 Oct
Discontinued Application: 62280

Drug Name

NYSTATIN AND TRIAMCINOLONE ACETONIDE

Product Number

2

Dosage Form

-

Strength

100,000 UNITS/GM;0.1%

Approval Date

1985-10-10

62280 / 2

Active Ingredient

NYSTATIN; TRIAMCINOLONE ACETONIDE

Application Number

62280

Product Number

2

Dosage Form

-

Strength

100,000 UNITS/GM;0.1%

Approval Date

1985-10-10

Regulatory Status

Discontinued

2001
20 Dec
Discontinued Application: 76090

Drug Name

PERMETHRIN

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

2001-12-20

76090 / 1

Active Ingredient

PERMETHRIN

Application Number

76090

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

2001-12-20

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85322

Drug Name

QUINIDINE SULFATE

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

85322 / 1

Active Ingredient

QUINIDINE SULFATE

Application Number

85322

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

2002
30 Aug
Discontinued Application: 76195

Drug Name

RANITIDINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 75MG BASE

Approval Date

2002-08-30

76195 / 1

Active Ingredient

RANITIDINE HYDROCHLORIDE

Application Number

76195

Product Number

1

Dosage Form

-

Strength

EQ 75MG BASE

Approval Date

2002-08-30

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84561

Drug Name

SECOBARBITAL SODIUM

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

84561 / 1

Active Ingredient

SECOBARBITAL SODIUM

Application Number

84561

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84560

Drug Name

SODIUM PENTOBARBITAL

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

84560 / 1

Active Ingredient

PENTOBARBITAL SODIUM

Application Number

84560

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1987
08 Dec
Discontinued Application: 72095

Drug Name

TAB-PROFEN

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1987-12-08

72095 / 1

Active Ingredient

IBUPROFEN

Application Number

72095

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1987-12-08

Regulatory Status

Discontinued

2009
30 Jul
Discontinued Application: 78104

Drug Name

TRIAMCINOLONE ACETONIDE

Product Number

1

Dosage Form

-

Strength

0.055MG/SPRAY

Approval Date

2009-07-30

78104 / 1

Active Ingredient

TRIAMCINOLONE ACETONIDE

Application Number

78104

Product Number

1

Dosage Form

-

Strength

0.055MG/SPRAY

Approval Date

2009-07-30

Regulatory Status

Discontinued

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Drug Status Breakdown
48 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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FDA Approved Drug Record Details Preview

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

Drug Name

ANTITUSSIVE

Application Number

71292

Product Number

1

Active Ingredient

DIPHENHYDRAMINE HYDROCHLORIDE

Dosage Form

-

Strength

12.5MG/5ML

FDA Approved Drug Data

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