Allergan Aesthetics
FDA Approved Drugs

Allergan Aesthetics

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 RX
  • Total Records 13
  • Latest Approval Date Jun 16, 2008
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
13
View
Discontinued
12
View
RX
1
View
Company Overview

Company

Allergan Aesthetics

Country

U.S.A

Website

Visit Website

Email

abbviecontractmfg@abbvie.com

Social Profiles

LinkedIn
Company Snapshot

Allergan Aesthetics

Irvine, California

U.S.A

www.allerganaesthetics.com/ abbviecontractmfg@abbvie.com View on Map
FDA Approved Drug Records ( 13 records )
1997
03 Nov
Discontinued Application: 20811

Drug Name

ACULAR PRESERVATIVE FREE

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

1997-11-03

20811 / 1

Active Ingredient

KETOROLAC TROMETHAMINE

Application Number

20811

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

1997-11-03

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80248

Drug Name

ALBALON

Product Number

1

Dosage Form

-

Strength

0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

80248 / 1

Active Ingredient

NAPHAZOLINE HYDROCHLORIDE

Application Number

80248

Product Number

1

Dosage Form

-

Strength

0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

Regulatory Status

Discontinued

1999
08 Dec
Discontinued Application: 21009

Drug Name

ALOCRIL

Product Number

1

Dosage Form

-

Strength

2% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1999-12-08

21009 / 1

Active Ingredient

NEDOCROMIL SODIUM

Application Number

21009

Product Number

1

Dosage Form

-

Strength

2% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1999-12-08

Regulatory Status

Discontinued

1997
13 Mar
Discontinued Application: 20490

Drug Name

ALPHAGAN

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

1997-03-13

20490 / 1

Active Ingredient

BRIMONIDINE TARTRATE

Application Number

20490

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

1997-03-13

Regulatory Status

Discontinued

1996
06 Sep
Discontinued Application: 20613

Drug Name

ALPHAGAN

Product Number

1

Dosage Form

-

Strength

0.2% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1996-09-06

20613 / 1

Active Ingredient

BRIMONIDINE TARTRATE

Application Number

20613

Product Number

1

Dosage Form

-

Strength

0.2% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1996-09-06

Regulatory Status

Discontinued

2003
16 Oct
Discontinued Application: 21565

Drug Name

ELESTAT

Product Number

1

Dosage Form

-

Strength

0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2003-10-16

21565 / 1

Active Ingredient

EPINASTINE HYDROCHLORIDE

Application Number

21565

Product Number

1

Dosage Form

-

Strength

0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2003-10-16

Regulatory Status

Discontinued

1993
30 Jul
RX Application: 19921

Drug Name

OCUFLOX

Product Number

1

Dosage Form

-

Strength

0.3%

Approval Date

1993-07-30

19921 / 1

Active Ingredient

OFLOXACIN

Application Number

19921

Product Number

1

Dosage Form

-

Strength

0.3%

Approval Date

1993-07-30

Regulatory Status

RX

1984
03 Oct
Discontinued Application: 18155

Drug Name

OPTICROM

Product Number

1

Dosage Form

-

Strength

4% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1984-10-03

18155 / 1

Active Ingredient

CROMOLYN SODIUM

Application Number

18155

Product Number

1

Dosage Form

-

Strength

4% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1984-10-03

Regulatory Status

Discontinued

1988
20 Oct
Discontinued Application: 50567

Drug Name

POLYTRIM

Product Number

1

Dosage Form

-

Strength

10,000 UNITS/ML;EQ 1MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1988-10-20

50567 / 1

Active Ingredient

POLYMYXIN B SULFATE; TRIMETHOPRIM SULFATE

Application Number

50567

Product Number

1

Dosage Form

-

Strength

10,000 UNITS/ML;EQ 1MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1988-10-20

Regulatory Status

Discontinued

2004
28 May
Discontinued Application: 21595

Drug Name

SANCTURA

Product Number

1

Dosage Form

-

Strength

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

Approval Date

2004-05-28

21595 / 1

Active Ingredient

TROSPIUM CHLORIDE

Application Number

21595

Product Number

1

Dosage Form

-

Strength

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

Approval Date

2004-05-28

Regulatory Status

Discontinued

2007
03 Aug
Discontinued Application: 22103

Drug Name

SANCTURA XR

Product Number

1

Dosage Form

-

Strength

60MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2007-08-03

22103 / 1

Active Ingredient

TROSPIUM CHLORIDE

Application Number

22103

Product Number

1

Dosage Form

-

Strength

60MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2007-08-03

Regulatory Status

Discontinued

2008
16 Jun
Discontinued Application: 22220

Drug Name

TRIVARIS

Product Number

1

Dosage Form

-

Strength

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

Approval Date

2008-06-16

22220 / 1

Active Ingredient

TRIAMCINOLONE ACETONIDE

Application Number

22220

Product Number

1

Dosage Form

-

Strength

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

Approval Date

2008-06-16

Regulatory Status

Discontinued

2003
28 Mar
Discontinued Application: 21493

Drug Name

ZYMAR

Product Number

1

Dosage Form

-

Strength

0.3% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2003-03-28

21493 / 1

Active Ingredient

GATIFLOXACIN

Application Number

21493

Product Number

1

Dosage Form

-

Strength

0.3% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2003-03-28

Regulatory Status

Discontinued

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  • FDA Approved Drugs Database
    13 View
Drug Status Breakdown
13 total
  • Discontinued
  • RX
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

ACULAR PRESERVATIVE FREE

Application Number

20811

Product Number

1

Active Ingredient

KETOROLAC TROMETHAMINE

Dosage Form

-

Strength

0.5%

FDA Approved Drug Data

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