Perrigo Company plc OTC
FDA Approved Drugs

Perrigo Company plc OTC

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.

OTC
  • Total Records 31
  • Latest Approval Date Mar 17, 2022
  • Data Source FDA
  • First Approval Date Dec 01, 1986
All
80
View
Unclassified
1
View
Discontinued
48
View
OTC
31
View
Company Overview

Company

Perrigo Company plc OTC

Country

Ireland

Website

Visit Website

Email

enquiries@pharmacompass.com

Social Profiles

LinkedIn X / Twitter
Company Snapshot

Perrigo Company plc OTC

The Sharp Building Hogan Place Dublin 2

Ireland

www.perrigo.com/ enquiries@pharmacompass.com View on Map
FDA Approved Drug Records ( 31 records )
1987
06 Apr
OTC Application: 70607

Drug Name

ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

120MG

Approval Date

1987-04-06

70607 / 1

Active Ingredient

ACETAMINOPHEN

Application Number

70607

Product Number

1

Dosage Form

-

Strength

120MG

Approval Date

1987-04-06

Regulatory Status

OTC

1986
01 Dec
OTC Application: 70608

Drug Name

ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

650MG

Approval Date

1986-12-01

70608 / 1

Active Ingredient

ACETAMINOPHEN

Application Number

70608

Product Number

1

Dosage Form

-

Strength

650MG

Approval Date

1986-12-01

Regulatory Status

OTC

2000
25 Feb
OTC Application: 75077

Drug Name

ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

650MG

Approval Date

2000-02-25

75077 / 1

Active Ingredient

ACETAMINOPHEN

Application Number

75077

Product Number

1

Dosage Form

-

Strength

650MG

Approval Date

2000-02-25

Regulatory Status

OTC

2001
26 Nov
OTC Application: 75794

Drug Name

ACETAMINOPHEN, ASPIRIN AND CAFFEINE

Product Number

1

Dosage Form

-

Strength

250MG;250MG;65MG

Approval Date

2001-11-26

75794 / 1

Active Ingredient

ACETAMINOPHEN; ASPIRIN; CAFFEINE

Application Number

75794

Product Number

1

Dosage Form

-

Strength

250MG;250MG;65MG

Approval Date

2001-11-26

Regulatory Status

OTC

2018
16 Nov
OTC Application: 210719

Drug Name

CETIRIZINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

5MG;120MG

Approval Date

2018-11-16

210719 / 1

Active Ingredient

CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE

Application Number

210719

Product Number

1

Dosage Form

-

Strength

5MG;120MG

Approval Date

2018-11-16

Regulatory Status

OTC

1998
22 Dec
OTC Application: 74937

Drug Name

CHILDRENS IBUPROFEN

Product Number

1

Dosage Form

-

Strength

100MG/5ML

Approval Date

1998-12-22

74937 / 1

Active Ingredient

IBUPROFEN

Application Number

74937

Product Number

1

Dosage Form

-

Strength

100MG/5ML

Approval Date

1998-12-22

Regulatory Status

OTC

2019
16 May
OTC Application: 211253

Drug Name

DICLOFENAC SODIUM

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

2019-05-16

211253 / 1

Active Ingredient

DICLOFENAC SODIUM

Application Number

211253

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

2019-05-16

Regulatory Status

OTC

1996
18 Sep
OTC Application: 40167

Drug Name

DOXYLAMINE SUCCINATE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1996-09-18

40167 / 1

Active Ingredient

DOXYLAMINE SUCCINATE

Application Number

40167

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1996-09-18

Regulatory Status

OTC

2005
18 Mar
OTC Application: 75400

Drug Name

FAMOTIDINE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2005-03-18

75400 / 1

Active Ingredient

FAMOTIDINE

Application Number

75400

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2005-03-18

Regulatory Status

OTC

1987
08 Dec
OTC Application: 72096

Drug Name

IBUPROFEN

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1987-12-08

72096 / 1

Active Ingredient

IBUPROFEN

Application Number

72096

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1987-12-08

Regulatory Status

OTC

2004
16 Jan
OTC Application: 76359

Drug Name

IBUPROFEN

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

2004-01-16

76359 / 2

Active Ingredient

IBUPROFEN

Application Number

76359

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

2004-01-16

Regulatory Status

OTC

2004
20 Aug
OTC Application: 75728

Drug Name

LORATADINE

Product Number

1

Dosage Form

-

Strength

1MG/ML

Approval Date

2004-08-20

75728 / 1

Active Ingredient

LORATADINE

Application Number

75728

Product Number

1

Dosage Form

-

Strength

1MG/ML

Approval Date

2004-08-20

Regulatory Status

OTC

2003
29 Sep
OTC Application: 76011

Drug Name

LORATADINE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2003-09-29

76011 / 1

Active Ingredient

LORATADINE

Application Number

76011

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2003-09-29

Regulatory Status

OTC

2004
25 Jun
OTC Application: 76301

Drug Name

LORATADINE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2004-06-25

76301 / 1

Active Ingredient

LORATADINE

Application Number

76301

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2004-06-25

Regulatory Status

OTC

2004
04 Mar
OTC Application: 75989

Drug Name

LORATADINE AND PSEUDOEPHEDRINE SULFATE

Product Number

1

Dosage Form

-

Strength

10MG;240MG

Approval Date

2004-03-04

75989 / 1

Active Ingredient

LORATADINE; PSEUDOEPHEDRINE SULFATE

Application Number

75989

Product Number

1

Dosage Form

-

Strength

10MG;240MG

Approval Date

2004-03-04

Regulatory Status

OTC

2003
30 Jan
OTC Application: 76050

Drug Name

LORATADINE AND PSEUDOEPHEDRINE SULFATE

Product Number

1

Dosage Form

-

Strength

5MG;120MG

Approval Date

2003-01-30

76050 / 1

Active Ingredient

LORATADINE; PSEUDOEPHEDRINE SULFATE

Application Number

76050

Product Number

1

Dosage Form

-

Strength

5MG;120MG

Approval Date

2003-01-30

Regulatory Status

OTC

2004
30 Mar
OTC Application: 76357

Drug Name

MICONAZOLE 3 COMBINATION PACK

Product Number

1

Dosage Form

-

Strength

2%,4%

Approval Date

2004-03-30

76357 / 1

Active Ingredient

MICONAZOLE NITRATE

Application Number

76357

Product Number

1

Dosage Form

-

Strength

2%,4%

Approval Date

2004-03-30

Regulatory Status

OTC

1997
15 May
OTC Application: 74760

Drug Name

MICONAZOLE NITRATE

Product Number

1

Dosage Form

-

Strength

2%

Approval Date

1997-05-15

74760 / 1

Active Ingredient

MICONAZOLE NITRATE

Application Number

74760

Product Number

1

Dosage Form

-

Strength

2%

Approval Date

1997-05-15

Regulatory Status

OTC

2011
28 Apr
OTC Application: 91344

Drug Name

MINOXIDIL

Product Number

1

Dosage Form

-

Strength

5%

Approval Date

2011-04-28

91344 / 1

Active Ingredient

MINOXIDIL

Application Number

91344

Product Number

1

Dosage Form

-

Strength

5%

Approval Date

2011-04-28

Regulatory Status

OTC

2001
13 Jun
OTC Application: 75598

Drug Name

MINOXIDIL EXTRA STRENGTH (FOR MEN)

Product Number

1

Dosage Form

-

Strength

5%

Approval Date

2001-06-13

75598 / 1

Active Ingredient

MINOXIDIL

Application Number

75598

Product Number

1

Dosage Form

-

Strength

5%

Approval Date

2001-06-13

Regulatory Status

OTC

1997
13 Jan
OTC Application: 74661

Drug Name

NAPROXEN SODIUM

Product Number

1

Dosage Form

-

Strength

220MG

Approval Date

1997-01-13

74661 / 1

Active Ingredient

NAPROXEN SODIUM

Application Number

74661

Product Number

1

Dosage Form

-

Strength

220MG

Approval Date

1997-01-13

Regulatory Status

OTC

2004
17 Mar
OTC Application: 76518

Drug Name

NAPROXEN SODIUM AND PSEUDOEPHEDRINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

220MG;120MG

Approval Date

2004-03-17

76518 / 1

Active Ingredient

NAPROXEN SODIUM; PSEUDOEPHEDRINE HYDROCHLORIDE

Application Number

76518

Product Number

1

Dosage Form

-

Strength

220MG;120MG

Approval Date

2004-03-17

Regulatory Status

OTC

2022
17 Mar
OTC Application: 215712

Drug Name

NASONEX 24HR ALLERGY

Product Number

1

Dosage Form

-

Strength

0.05MG/SPRAY

Approval Date

2022-03-17

215712 / 1

Active Ingredient

MOMETASONE FUROATE

Application Number

215712

Product Number

1

Dosage Form

-

Strength

0.05MG/SPRAY

Approval Date

2022-03-17

Regulatory Status

OTC

2009
10 Jul
OTC Application: 90711

Drug Name

NICOTINE POLACRILEX

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE

Approval Date

2009-07-10

90711 / 1

Active Ingredient

NICOTINE POLACRILEX

Application Number

90711

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE

Approval Date

2009-07-10

Regulatory Status

OTC

2009
10 Jul
OTC Application: 90711

Drug Name

NICOTINE POLACRILEX

Product Number

2

Dosage Form

-

Strength

EQ 4MG BASE

Approval Date

2009-07-10

90711 / 2

Active Ingredient

NICOTINE POLACRILEX

Application Number

90711

Product Number

2

Dosage Form

-

Strength

EQ 4MG BASE

Approval Date

2009-07-10

Regulatory Status

OTC

2012
09 Oct
OTC Application: 203690

Drug Name

NICOTINE POLACRILEX

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE

Approval Date

2012-10-09

203690 / 1

Active Ingredient

NICOTINE POLACRILEX

Application Number

203690

Product Number

1

Dosage Form

-

Strength

EQ 2MG BASE

Approval Date

2012-10-09

Regulatory Status

OTC

2012
09 Oct
OTC Application: 203690

Drug Name

NICOTINE POLACRILEX

Product Number

2

Dosage Form

-

Strength

EQ 4MG BASE

Approval Date

2012-10-09

203690 / 2

Active Ingredient

NICOTINE POLACRILEX

Application Number

203690

Product Number

2

Dosage Form

-

Strength

EQ 4MG BASE

Approval Date

2012-10-09

Regulatory Status

OTC

2009
06 Oct
OTC Application: 90685

Drug Name

POLYETHYLENE GLYCOL 3350

Product Number

1

Dosage Form

-

Strength

17GM/PACKET

Approval Date

2009-10-06

90685 / 1

Active Ingredient

POLYETHYLENE GLYCOL 3350

Application Number

90685

Product Number

1

Dosage Form

-

Strength

17GM/PACKET

Approval Date

2009-10-06

Regulatory Status

OTC

2009
06 Oct
OTC Application: 90685

Drug Name

POLYETHYLENE GLYCOL 3350

Product Number

2

Dosage Form

-

Strength

17GM/SCOOPFUL

Approval Date

2009-10-06

90685 / 2

Active Ingredient

POLYETHYLENE GLYCOL 3350

Application Number

90685

Product Number

2

Dosage Form

-

Strength

17GM/SCOOPFUL

Approval Date

2009-10-06

Regulatory Status

OTC

2001
21 Nov
OTC Application: 75915

Drug Name

TIOCONAZOLE

Product Number

1

Dosage Form

-

Strength

6.5%

Approval Date

2001-11-21

75915 / 1

Active Ingredient

TIOCONAZOLE

Application Number

75915

Product Number

1

Dosage Form

-

Strength

6.5%

Approval Date

2001-11-21

Regulatory Status

OTC

2014
14 Nov
OTC Application: 78104

Drug Name

TRIAMCINOLONE ACETONIDE

Product Number

2

Dosage Form

-

Strength

0.055MG/SPRAY

Approval Date

2014-11-14

78104 / 2

Active Ingredient

TRIAMCINOLONE ACETONIDE

Application Number

78104

Product Number

2

Dosage Form

-

Strength

0.055MG/SPRAY

Approval Date

2014-11-14

Regulatory Status

OTC

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Drug Status Breakdown
31 total
  • OTC
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

ACETAMINOPHEN

Application Number

70607

Product Number

1

Active Ingredient

ACETAMINOPHEN

Dosage Form

-

Strength

120MG

FDA Approved Drug Data

Approved drug product information

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