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Allergan Aesthetics
FDA Orange Book

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Allergan Aesthetics Presents Repeat Trenibote Safety Data

30 Mar 2026

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Allergan Aesthetics Unveils Evolved Approach via Global Survey

19 Mar 2026

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Allergan Aesthetics Launches Index to Redefine Skin Quality

16 Mar 2026

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Allergan Aesthetics

VIRTUAL BOOTH, Contact Details

VIRTUAL BOOTH
CONTACT DETAILS
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EVENTS

Webinars & Exhibitions

Webinars & Exhibitions

DIGITAL CONTENT

1518 News #PharmaBuzz

1518 News #PharmaBuzz

ACTIVE PHARMA INGREDIENTS

2 All APIs, 2 NDC API

2 All APIs
2 NDC API

DEVELOPMENTS

83 Drugs in Development

83 Drugs in Development

FINISHED DOSAGE FORMULATIONS

152 FDF Dossiers, 99 FDA Orange Book, 46 Europe, 3 Canada, 4 South Africa

152 FDF Dossiers
99 FDA Orange Book
46 Europe
3 Canada
4 South Africa

INSPECTIONS & REGISTRATIONS

49 FDA, 6 EDQM, 2 GDUFA

49 FDA
6 EDQM
2 GDUFA

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filter Active Ingredients Reset all filters

99 All

01 2ASPIRIN; BUTALBITAL; CAFFEINE

02 1ASPIRIN; BUTALBITAL; CAFFEINE; CODEINE PHOSPHATE

03 2BRIMONIDINE TARTRATE

04 2CHLORAMPHENICOL

05 1CHLORAMPHENICOL; PREDNISOLONE

06 1CROMOLYN SODIUM

07 1CYCLOSPORINE

08 1DEXAMETHASONE

09 2DICYCLOMINE HYDROCHLORIDE

10 3DILTIAZEM HYDROCHLORIDE

11 1DIPIVEFRIN HYDROCHLORIDE

12 1EPINASTINE HYDROCHLORIDE

13 4ETHINYL ESTRADIOL; NORETHINDRONE

14 1ETHOXZOLAMIDE

15 4FLUOCINOLONE ACETONIDE

16 1FLUOROMETHOLONE

17 1FLUOROMETHOLONE; SULFACETAMIDE SODIUM

18 1FLURBIPROFEN SODIUM

19 1GATIFLOXACIN

20 1GENTAMICIN SULFATE

21 2GENTAMICIN SULFATE; PREDNISOLONE ACETATE

22 5HYDROCORTISONE

23 2HYDROXYPROGESTERONE CAPROATE

24 1IDOXURIDINE

25 1IRON DEXTRAN

26 1KETOROLAC TROMETHAMINE

27 2LEVOBUNOLOL HYDROCHLORIDE

28 6LIOTRIX (T4;T3)

29 1MEDRYSONE

30 1MEMANTINE HYDROCHLORIDE

31 12MORPHINE SULFATE

32 1NAPHAZOLINE HYDROCHLORIDE

33 4NEBIVOLOL HYDROCHLORIDE

34 1NEDOCROMIL SODIUM

35 1NEOMYCIN SULFATE; POLYMYXIN B SULFATE; PREDNISOLONE ACETATE

36 1OFLOXACIN

37 2OXYBUTYNIN

38 5OnabotulinumtoxinA

39 1PHENYLEPHRINE HYDROCHLORIDE; PYRILAMINE MALEATE

40 1PODOFILOX

41 1POLYMYXIN B SULFATE; TRIMETHOPRIM SULFATE

42 2PREDNISOLONE ACETATE; SULFACETAMIDE SODIUM

43 1PROPARACAINE HYDROCHLORIDE

44 1SELENIUM SULFIDE

45 3SULFACETAMIDE SODIUM

46 2TRETINOIN

47 1TRIAMCINOLONE ACETONIDE

48 3TRIMEPRAZINE TARTRATE

49 2TROSPIUM CHLORIDE

filter Dosage Reset all filters

99 All

01 2AEROSOL;TOPICAL

02 17CAPSULE, EXTENDED RELEASE;ORAL

03 3CAPSULE;ORAL

04 4CREAM;TOPICAL

05 1EMULSION; OPHTHALMIC

06 1FILM, EXTENDED RELEASE;TRANSDERMAL

07 1GEL, METERED;TRANSDERMAL

08 3GEL;TOPICAL

09 3INJECTABLE;INJECTION

10 1INJECTABLE;INTRA-ARTICULAR, INTRAMUSCULAR, INTRAVITREAL

11 1LOTION/SHAMPOO;TOPICAL

12 6OINTMENT;OPHTHALMIC

13 2OINTMENT;TOPICAL

14 21SOLUTION/DROPS;OPHTHALMIC

15 1SOLUTION;ORAL

16 2SOLUTION;TOPICAL

17 3SUSPENSION/DROPS;OPHTHALMIC

18 2SUSPENSION;OPHTHALMIC

19 1SYRUP;ORAL

20 15TABLET;ORAL

21 2TABLET;ORAL-21

22 2TABLET;ORAL-28

23 5VIAL; SINGLE-USE

filter Dosage Strength Reset all filters

99 All

01 10.01%

02 10.01% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

03 10.0125MG;0.0031MG

04 30.025%

05 10.025MG;0.0063MG

06 10.03% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

07 20.035MG;0.5MG

08 20.035MG;1MG

09 10.0375%

10 10.05%

11 10.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

12 10.05MG;0.0125MG

13 10.075%

14 30.1%

15 10.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

16 10.1%;10%

17 10.12%;0.1%

18 10.15MG;0.0375MG

19 10.1MG;0.025MG

20 10.2% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

21 20.2%;10%

22 10.25% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

23 10.25MG;0.0625MG

24 10.3%

25 10.3% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

26 60.5%

27 10.5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

28 51%

29 11%;0.5%

30 210%

31 110,000 UNITS/ML;EQ 1MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

32 2100 UNITS/VIAL

33 1100MG

34 110MG

35 110MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

36 1120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

37 1125MG

38 1125MG/ML

39 1130MG

40 1150MG

41 1180MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

42 12% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

43 22.5%

44 1200 UNITS/VIAL

45 1200MG

46 120MG

47 220MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

48 1240MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

49 1250MG/ML

50 12MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

51 13%

52 13.9MG/24HR

53 130%

54 130MG

55 2325MG;50MG;40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

56 1325MG;50MG;40MG;30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

57 14% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

58 140MG

59 250 UNITS/VIAL

60 150MG

61 160MG

62 160MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

63 170MG

64 180MG

65 18MG/0.1ML (8MG/0.1ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

66 1EQ 0.3% BASE

67 1EQ 0.3% BASE;0.6%

68 1EQ 0.3% BASE;1%

69 1EQ 0.35% BASE;10,000 UNITS/ML;0.5%

70 1EQ 100MG IRON/2ML (EQ 50MG IRON/ML)

71 1EQ 10MG BASE

72 2EQ 2.5MG BASE

73 1EQ 2.5MG BASE/5ML

74 1EQ 20MG BASE

75 2EQ 5MG BASE

filter Regulatory Info Reset all filters

99 All

01 85DISCN

02 8RX

03 6Blank

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01

Brand Name : FIORINAL

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RLD : Yes

TE Code :

ASPIRIN; BUTALBITAL; CAFFEINE

Allergan Aesthetics

Dosage Form : TABLET; ORAL

Proprietary Name : FIORINAL

Dosage Strength : 325MG;50MG;40MG **Federa...

Approval Date : 1986-04-16

Application Number : 17534

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Product
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02

Brand Name : FIORINAL

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Ireland

Digital Content

RLD : Yes

TE Code :

ASPIRIN; BUTALBITAL; CAFFEINE

Allergan Aesthetics

Dosage Form : CAPSULE; ORAL

Proprietary Name : FIORINAL

Dosage Strength : 325MG;50MG;40MG **Federa...

Approval Date : 1986-04-16

Application Number : 17534

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Product
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03

Brand Name : FIORINAL W/CODEINE

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Digital Content

RLD : Yes

TE Code :

ASPIRIN; BUTALBITAL; CAFFEINE; CODEINE PHOSPHATE

Allergan Aesthetics

Dosage Form : CAPSULE; ORAL

Proprietary Name : FIORINAL W/CODEINE

Dosage Strength : 325MG;50MG;40MG;30MG **F...

Approval Date : 1990-10-26

Application Number : 19429

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Product
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04

Brand Name : ALPHAGAN

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Ireland

Digital Content

RLD : No

TE Code :

BRIMONIDINE TARTRATE

Allergan Aesthetics

Dosage Form : SOLUTION/DROPS; OPHTHALMIC

Proprietary Name : ALPHAGAN

Dosage Strength : 0.5%

Approval Date : 1997-03-13

Application Number : 20490

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Product
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05

Brand Name : ALPHAGAN

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RLD : Yes

TE Code :

BRIMONIDINE TARTRATE

Allergan Aesthetics

Dosage Form : SOLUTION/DROPS; OPHTHALMIC

Proprietary Name : ALPHAGAN

Dosage Strength : 0.2% **Federal Register ...

Approval Date : 1996-09-06

Application Number : 20613

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Product
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06

Brand Name : CHLOROPTIC

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RLD : No

TE Code :

CHLORAMPHENICOL

Allergan Aesthetics

Dosage Form : SOLUTION/DROPS; OPHTHALMIC

Proprietary Name : CHLOROPTIC

Dosage Strength : 0.5%

Approval Date : 1982-01-01

Application Number : 50091

RX/OTC/DISCN : DISCN

RLD : No

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Product
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07

Brand Name : CHLOROPTIC S.O.P.

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RLD : No

TE Code :

CHLORAMPHENICOL

Allergan Aesthetics

Dosage Form : OINTMENT; OPHTHALMIC

Proprietary Name : CHLOROPTIC S.O.P.

Dosage Strength : 1%

Approval Date : 1982-01-01

Application Number : 61187

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Product
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08

Brand Name : CHLOROPTIC-P S.O.P.

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RLD : No

TE Code :

CHLORAMPHENICOL; PREDNISOLONE

Allergan Aesthetics

Dosage Form : OINTMENT; OPHTHALMIC

Proprietary Name : CHLOROPTIC-P S.O.P.

Dosage Strength : 1%;0.5%

Approval Date : 1982-01-01

Application Number : 61188

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Product
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09

Brand Name : OPTICROM

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RLD : Yes

TE Code :

CROMOLYN SODIUM

Allergan Aesthetics

Dosage Form : SOLUTION/DROPS; OPHTHALMIC

Proprietary Name : OPTICROM

Dosage Strength : 4% **Federal Register de...

Approval Date : 1984-10-03

Application Number : 18155

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

Product
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10

Brand Name : RESTASIS

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RLD :

TE Code :

CYCLOSPORINE

Allergan Aesthetics

Dosage Form : EMULSION; OPHTHALMIC

Proprietary Name : RESTASIS

Dosage Strength : 0.05%

Approval Date :

Application Number : 21023

RX/OTC/DISCN :

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