Bausch & Lomb Incorporated Discontinued
FDA Approved Drugs

Bausch & Lomb Incorporated 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 87
  • Latest Approval Date Apr 08, 2005
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
114
View
Unclassified
2
View
Discontinued
87
View
OTC
4
View
RX
21
View
Company Overview

Company

Bausch & Lomb Incorporated Discontinued

Country

Canada

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Company Snapshot

Bausch & Lomb Incorporated Discontinued

520 Applewood Crescent, Vaughan, Ontario, Canada L4K 4B4

Canada

www.bausch.com/ View on Map
FDA Approved Drug Records ( 87 records )
1994
25 Feb
Discontinued Application: 40063

Drug Name

ACETIC ACID 2% IN AQUEOUS ALUMINUM ACETATE

Product Number

1

Dosage Form

-

Strength

2%;0.79%

Approval Date

1994-02-25

40063 / 1

Active Ingredient

ACETIC ACID, GLACIAL; ALUMINUM ACETATE

Application Number

40063

Product Number

1

Dosage Form

-

Strength

2%;0.79%

Approval Date

1994-02-25

Regulatory Status

Discontinued

1984
28 Mar
Discontinued Application: 62453

Drug Name

BACITRACIN

Product Number

1

Dosage Form

-

Strength

500 UNITS/GM

Approval Date

1984-03-28

62453 / 1

Active Ingredient

BACITRACIN

Application Number

62453

Product Number

1

Dosage Form

-

Strength

500 UNITS/GM

Approval Date

1984-03-28

Regulatory Status

Discontinued

1982
09 Sep
Discontinued Application: 62386

Drug Name

BACITRACIN ZINC-NEOMYCIN SULFATE-POLYMYXIN B SULFATE

Product Number

1

Dosage Form

-

Strength

400 UNITS/GM;EQ 3.5MG BASE/GM;10,000 UNITS/GM

Approval Date

1982-09-09

62386 / 1

Active Ingredient

BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

Application Number

62386

Product Number

1

Dosage Form

-

Strength

400 UNITS/GM;EQ 3.5MG BASE/GM;10,000 UNITS/GM

Approval Date

1982-09-09

Regulatory Status

Discontinued

1987
29 May
Discontinued Application: 70484

Drug Name

BETAMETHASONE VALERATE

Product Number

1

Dosage Form

-

Strength

EQ 0.1% BASE

Approval Date

1987-05-29

70484 / 1

Active Ingredient

BETAMETHASONE VALERATE

Application Number

70484

Product Number

1

Dosage Form

-

Strength

EQ 0.1% BASE

Approval Date

1987-05-29

Regulatory Status

Discontinued

1987
29 May
Discontinued Application: 70485

Drug Name

BETAMETHASONE VALERATE

Product Number

1

Dosage Form

-

Strength

EQ 0.1% BASE

Approval Date

1987-05-29

70485 / 1

Active Ingredient

BETAMETHASONE VALERATE

Application Number

70485

Product Number

1

Dosage Form

-

Strength

EQ 0.1% BASE

Approval Date

1987-05-29

Regulatory Status

Discontinued

1987
29 May
Discontinued Application: 70486

Drug Name

BETAMETHASONE VALERATE

Product Number

1

Dosage Form

-

Strength

EQ 0.1% BASE

Approval Date

1987-05-29

70486 / 1

Active Ingredient

BETAMETHASONE VALERATE

Application Number

70486

Product Number

1

Dosage Form

-

Strength

EQ 0.1% BASE

Approval Date

1987-05-29

Regulatory Status

Discontinued

1985
21 Aug
Discontinued Application: 88606

Drug Name

BOROFAIR

Product Number

1

Dosage Form

-

Strength

2%;0.79%

Approval Date

1985-08-21

88606 / 1

Active Ingredient

ACETIC ACID, GLACIAL; ALUMINUM ACETATE

Application Number

88606

Product Number

1

Dosage Form

-

Strength

2%;0.79%

Approval Date

1985-08-21

Regulatory Status

Discontinued

1986
21 May
Discontinued Application: 70292

Drug Name

CARBACHOL

Product Number

1

Dosage Form

-

Strength

0.01%

Approval Date

1986-05-21

70292 / 1

Active Ingredient

CARBACHOL

Application Number

70292

Product Number

1

Dosage Form

-

Strength

0.01%

Approval Date

1986-05-21

Regulatory Status

Discontinued

2000
20 Jan
Discontinued Application: 75546

Drug Name

CARTEOLOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

2000-01-20

75546 / 1

Active Ingredient

CARTEOLOL HYDROCHLORIDE

Application Number

75546

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

2000-01-20

Regulatory Status

Discontinued

1983
14 Apr
Discontinued Application: 62437

Drug Name

CHLOROFAIR

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

1983-04-14

62437 / 1

Active Ingredient

CHLORAMPHENICOL

Application Number

62437

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

1983-04-14

Regulatory Status

Discontinued

1983
21 Apr
Discontinued Application: 62439

Drug Name

CHLOROFAIR

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1983-04-21

62439 / 1

Active Ingredient

CHLORAMPHENICOL

Application Number

62439

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1983-04-21

Regulatory Status

Discontinued

1995
30 Jan
Discontinued Application: 74443

Drug Name

CROLOM

Product Number

1

Dosage Form

-

Strength

4%

Approval Date

1995-01-30

74443 / 1

Active Ingredient

CROMOLYN SODIUM

Application Number

74443

Product Number

1

Dosage Form

-

Strength

4%

Approval Date

1995-01-30

Regulatory Status

Discontinued

1982
28 Dec
Discontinued Application: 88071

Drug Name

DEXAIR

Product Number

1

Dosage Form

-

Strength

EQ 0.05% PHOSPHATE

Approval Date

1982-12-28

88071 / 1

Active Ingredient

DEXAMETHASONE SODIUM PHOSPHATE

Application Number

88071

Product Number

1

Dosage Form

-

Strength

EQ 0.05% PHOSPHATE

Approval Date

1982-12-28

Regulatory Status

Discontinued

1983
15 Dec
Discontinued Application: 88433

Drug Name

DEXAIR

Product Number

1

Dosage Form

-

Strength

EQ 0.1% PHOSPHATE

Approval Date

1983-12-15

88433 / 1

Active Ingredient

DEXAMETHASONE SODIUM PHOSPHATE

Application Number

88433

Product Number

1

Dosage Form

-

Strength

EQ 0.1% PHOSPHATE

Approval Date

1983-12-15

Regulatory Status

Discontinued

1983
16 May
Discontinued Application: 62411

Drug Name

DEXASPORIN

Product Number

1

Dosage Form

-

Strength

0.1%;EQ 3.5MG BASE/GM;10,000 UNITS/GM

Approval Date

1983-05-16

62411 / 1

Active Ingredient

DEXAMETHASONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

Application Number

62411

Product Number

1

Dosage Form

-

Strength

0.1%;EQ 3.5MG BASE/GM;10,000 UNITS/GM

Approval Date

1983-05-16

Regulatory Status

Discontinued

1983
18 May
Discontinued Application: 62428

Drug Name

DEXASPORIN

Product Number

1

Dosage Form

-

Strength

0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML

Approval Date

1983-05-18

62428 / 1

Active Ingredient

DEXAMETHASONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

Application Number

62428

Product Number

1

Dosage Form

-

Strength

0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML

Approval Date

1983-05-18

Regulatory Status

Discontinued

1995
19 May
Discontinued Application: 74188

Drug Name

DIPIVEFRIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

1995-05-19

74188 / 1

Active Ingredient

DIPIVEFRIN HYDROCHLORIDE

Application Number

74188

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

1995-05-19

Regulatory Status

Discontinued

1984
05 Apr
Discontinued Application: 62481

Drug Name

ERYTHROMYCIN

Product Number

1

Dosage Form

-

Strength

5MG/GM

Approval Date

1984-04-05

62481 / 1

Active Ingredient

ERYTHROMYCIN

Application Number

62481

Product Number

1

Dosage Form

-

Strength

5MG/GM

Approval Date

1984-04-05

Regulatory Status

Discontinued

1984
11 Jul
Discontinued Application: 62485

Drug Name

ERYTHROMYCIN

Product Number

1

Dosage Form

-

Strength

1.5%

Approval Date

1984-07-11

62485 / 1

Active Ingredient

ERYTHROMYCIN

Application Number

62485

Product Number

1

Dosage Form

-

Strength

1.5%

Approval Date

1984-07-11

Regulatory Status

Discontinued

1985
25 Jul
Discontinued Application: 62616

Drug Name

ERYTHROMYCIN

Product Number

1

Dosage Form

-

Strength

2%

Approval Date

1985-07-25

62616 / 1

Active Ingredient

ERYTHROMYCIN

Application Number

62616

Product Number

1

Dosage Form

-

Strength

2%

Approval Date

1985-07-25

Regulatory Status

Discontinued

1985
15 Mar
Discontinued Application: 62558

Drug Name

ERYTHROMYCIN ETHYLSUCCINATE

Product Number

1

Dosage Form

-

Strength

EQ 400MG BASE/5ML

Approval Date

1985-03-15

62558 / 1

Active Ingredient

ERYTHROMYCIN ETHYLSUCCINATE

Application Number

62558

Product Number

1

Dosage Form

-

Strength

EQ 400MG BASE/5ML

Approval Date

1985-03-15

Regulatory Status

Discontinued

1985
15 Mar
Discontinued Application: 62559

Drug Name

ERYTHROMYCIN ETHYLSUCCINATE

Product Number

1

Dosage Form

-

Strength

EQ 200MG BASE/5ML

Approval Date

1985-03-15

62559 / 1

Active Ingredient

ERYTHROMYCIN ETHYLSUCCINATE

Application Number

62559

Product Number

1

Dosage Form

-

Strength

EQ 200MG BASE/5ML

Approval Date

1985-03-15

Regulatory Status

Discontinued

1993
20 Dec
Discontinued Application: 40059

Drug Name

FLUOCINOLONE ACETONIDE

Product Number

1

Dosage Form

-

Strength

0.01%

Approval Date

1993-12-20

40059 / 1

Active Ingredient

FLUOCINOLONE ACETONIDE

Application Number

40059

Product Number

1

Dosage Form

-

Strength

0.01%

Approval Date

1993-12-20

Regulatory Status

Discontinued

1984
08 Feb
Discontinued Application: 88449

Drug Name

FLUOCINOLONE ACETONIDE

Product Number

1

Dosage Form

-

Strength

0.01%

Approval Date

1984-02-08

88449 / 1

Active Ingredient

FLUOCINOLONE ACETONIDE

Application Number

88449

Product Number

1

Dosage Form

-

Strength

0.01%

Approval Date

1984-02-08

Regulatory Status

Discontinued

1984
02 Aug
Discontinued Application: 88499

Drug Name

FLUOCINOLONE ACETONIDE

Product Number

1

Dosage Form

-

Strength

0.01%

Approval Date

1984-08-02

88499 / 1

Active Ingredient

FLUOCINOLONE ACETONIDE

Application Number

88499

Product Number

1

Dosage Form

-

Strength

0.01%

Approval Date

1984-08-02

Regulatory Status

Discontinued

1984
02 Aug
Discontinued Application: 88506

Drug Name

FLUOCINOLONE ACETONIDE

Product Number

1

Dosage Form

-

Strength

0.025%

Approval Date

1984-08-02

88506 / 1

Active Ingredient

FLUOCINOLONE ACETONIDE

Application Number

88506

Product Number

1

Dosage Form

-

Strength

0.025%

Approval Date

1984-08-02

Regulatory Status

Discontinued

1984
27 Feb
Discontinued Application: 88507

Drug Name

FLUOCINOLONE ACETONIDE

Product Number

1

Dosage Form

-

Strength

0.025%

Approval Date

1984-02-27

88507 / 1

Active Ingredient

FLUOCINOLONE ACETONIDE

Application Number

88507

Product Number

1

Dosage Form

-

Strength

0.025%

Approval Date

1984-02-27

Regulatory Status

Discontinued

1983
03 May
Discontinued Application: 62440

Drug Name

GENTAFAIR

Product Number

1

Dosage Form

-

Strength

EQ 0.3% BASE

Approval Date

1983-05-03

62440 / 1

Active Ingredient

GENTAMICIN SULFATE

Application Number

62440

Product Number

1

Dosage Form

-

Strength

EQ 0.3% BASE

Approval Date

1983-05-03

Regulatory Status

Discontinued

1983
26 May
Discontinued Application: 62443

Drug Name

GENTAFAIR

Product Number

1

Dosage Form

-

Strength

EQ 3MG BASE/GM

Approval Date

1983-05-26

62443 / 1

Active Ingredient

GENTAMICIN SULFATE

Application Number

62443

Product Number

1

Dosage Form

-

Strength

EQ 3MG BASE/GM

Approval Date

1983-05-26

Regulatory Status

Discontinued

1983
26 May
Discontinued Application: 62444

Drug Name

GENTAFAIR

Product Number

1

Dosage Form

-

Strength

EQ 0.1% BASE

Approval Date

1983-05-26

62444 / 1

Active Ingredient

GENTAMICIN SULFATE

Application Number

62444

Product Number

1

Dosage Form

-

Strength

EQ 0.1% BASE

Approval Date

1983-05-26

Regulatory Status

Discontinued

1983
01 Sep
Discontinued Application: 62458

Drug Name

GENTAFAIR

Product Number

1

Dosage Form

-

Strength

EQ 0.1% BASE

Approval Date

1983-09-01

62458 / 1

Active Ingredient

GENTAMICIN SULFATE

Application Number

62458

Product Number

1

Dosage Form

-

Strength

EQ 0.1% BASE

Approval Date

1983-09-01

Regulatory Status

Discontinued

1985
28 Aug
Discontinued Application: 62493

Drug Name

GENTAFAIR

Product Number

1

Dosage Form

-

Strength

EQ 40MG BASE/ML

Approval Date

1985-08-28

62493 / 1

Active Ingredient

GENTAMICIN SULFATE

Application Number

62493

Product Number

1

Dosage Form

-

Strength

EQ 40MG BASE/ML

Approval Date

1985-08-28

Regulatory Status

Discontinued

1982
28 Jul
Discontinued Application: 87838

Drug Name

HYDROCORTISONE

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-07-28

87838 / 1

Active Ingredient

HYDROCORTISONE

Application Number

87838

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-07-28

Regulatory Status

Discontinued

1994
31 Oct
Discontinued Application: 40097

Drug Name

HYDROCORTISONE AND ACETIC ACID

Product Number

1

Dosage Form

-

Strength

2%;1%

Approval Date

1994-10-31

40097 / 1

Active Ingredient

ACETIC ACID, GLACIAL; HYDROCORTISONE

Application Number

40097

Product Number

1

Dosage Form

-

Strength

2%;1%

Approval Date

1994-10-31

Regulatory Status

Discontinued

1986
14 Feb
Discontinued Application: 88862

Drug Name

HYDROXYZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG/ML

Approval Date

1986-02-14

88862 / 1

Active Ingredient

HYDROXYZINE HYDROCHLORIDE

Application Number

88862

Product Number

1

Dosage Form

-

Strength

25MG/ML

Approval Date

1986-02-14

Regulatory Status

Discontinued

1986
14 Feb
Discontinued Application: 88881

Drug Name

HYDROXYZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

50MG/ML

Approval Date

1986-02-14

88881 / 1

Active Ingredient

HYDROXYZINE HYDROCHLORIDE

Application Number

88881

Product Number

1

Dosage Form

-

Strength

50MG/ML

Approval Date

1986-02-14

Regulatory Status

Discontinued

1986
14 Feb
Discontinued Application: 89106

Drug Name

HYDROXYZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG/ML

Approval Date

1986-02-14

89106 / 1

Active Ingredient

HYDROXYZINE HYDROCHLORIDE

Application Number

89106

Product Number

1

Dosage Form

-

Strength

25MG/ML

Approval Date

1986-02-14

Regulatory Status

Discontinued

1986
14 Feb
Discontinued Application: 89107

Drug Name

HYDROXYZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

50MG/ML

Approval Date

1986-02-14

89107 / 1

Active Ingredient

HYDROXYZINE HYDROCHLORIDE

Application Number

89107

Product Number

1

Dosage Form

-

Strength

50MG/ML

Approval Date

1986-02-14

Regulatory Status

Discontinued

1983
07 Jun
Discontinued Application: 88087

Drug Name

KAINAIR

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

1983-06-07

88087 / 1

Active Ingredient

PROPARACAINE HYDROCHLORIDE

Application Number

88087

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

1983-06-07

Regulatory Status

Discontinued

1987
07 May
Discontinued Application: 62668

Drug Name

KANAMYCIN SULFATE

Product Number

1

Dosage Form

-

Strength

EQ 75MG BASE/2ML

Approval Date

1987-05-07

62668 / 1

Active Ingredient

KANAMYCIN SULFATE

Application Number

62668

Product Number

1

Dosage Form

-

Strength

EQ 75MG BASE/2ML

Approval Date

1987-05-07

Regulatory Status

Discontinued

1987
07 May
Discontinued Application: 62669

Drug Name

KANAMYCIN SULFATE

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/3ML

Approval Date

1987-05-07

62669 / 1

Active Ingredient

KANAMYCIN SULFATE

Application Number

62669

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/3ML

Approval Date

1987-05-07

Regulatory Status

Discontinued

1987
07 May
Discontinued Application: 62672

Drug Name

KANAMYCIN SULFATE

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/2ML

Approval Date

1987-05-07

62672 / 1

Active Ingredient

KANAMYCIN SULFATE

Application Number

62672

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/2ML

Approval Date

1987-05-07

Regulatory Status

Discontinued

1994
04 Mar
Discontinued Application: 74307

Drug Name

LEVOBUNOLOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

0.25%

Approval Date

1994-03-04

74307 / 1

Active Ingredient

LEVOBUNOLOL HYDROCHLORIDE

Application Number

74307

Product Number

1

Dosage Form

-

Strength

0.25%

Approval Date

1994-03-04

Regulatory Status

Discontinued

1996
09 Apr
Discontinued Application: 74643

Drug Name

MINOXIDIL (FOR MEN)

Product Number

1

Dosage Form

-

Strength

2%

Approval Date

1996-04-09

74643 / 1

Active Ingredient

MINOXIDIL

Application Number

74643

Product Number

1

Dosage Form

-

Strength

2%

Approval Date

1996-04-09

Regulatory Status

Discontinued

1983
16 Sep
Discontinued Application: 88230

Drug Name

MYDRIAFAIR

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1983-09-16

88230 / 1

Active Ingredient

TROPICAMIDE

Application Number

88230

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1983-09-16

Regulatory Status

Discontinued

1983
16 Sep
Discontinued Application: 88274

Drug Name

MYDRIAFAIR

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

1983-09-16

88274 / 1

Active Ingredient

TROPICAMIDE

Application Number

88274

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

1983-09-16

Regulatory Status

Discontinued

1994
25 May
Discontinued Application: 40073

Drug Name

NAFAZAIR

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

1994-05-25

40073 / 1

Active Ingredient

NAPHAZOLINE HYDROCHLORIDE

Application Number

40073

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

1994-05-25

Regulatory Status

Discontinued

1983
15 Apr
Discontinued Application: 88101

Drug Name

NAFAZAIR

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

1983-04-15

88101 / 1

Active Ingredient

NAPHAZOLINE HYDROCHLORIDE

Application Number

88101

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

1983-04-15

Regulatory Status

Discontinued

1985
06 Sep
Discontinued Application: 62381

Drug Name

NEOMYCIN & POLYMYXIN B SULFATES & BACITRACIN ZINC & HYDROCORTISONE

Product Number

1

Dosage Form

-

Strength

400 UNITS/GM;1%;EQ 3.5MG BASE/GM;5,000 UNITS/GM

Approval Date

1985-09-06

62381 / 1

Active Ingredient

BACITRACIN ZINC; HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

Application Number

62381

Product Number

1

Dosage Form

-

Strength

400 UNITS/GM;1%;EQ 3.5MG BASE/GM;5,000 UNITS/GM

Approval Date

1985-09-06

Regulatory Status

Discontinued

1995
30 Oct
Discontinued Application: 64055

Drug Name

NEOMYCIN SULFATE AND DEXAMETHASONE SODIUM PHOSPHATE

Product Number

1

Dosage Form

-

Strength

EQ 0.1% PHOSPHATE;EQ 3.5MG BASE/ML

Approval Date

1995-10-30

64055 / 1

Active Ingredient

DEXAMETHASONE SODIUM PHOSPHATE; NEOMYCIN SULFATE

Application Number

64055

Product Number

1

Dosage Form

-

Strength

EQ 0.1% PHOSPHATE;EQ 3.5MG BASE/ML

Approval Date

1995-10-30

Regulatory Status

Discontinued

1982
31 Aug
Discontinued Application: 62383

Drug Name

NEOMYCIN SULFATE AND POLYMYXIN B SULFATE GRAMICIDIN

Product Number

1

Dosage Form

-

Strength

0.025MG/ML;EQ 1.75MG BASE/ML;10,000 UNITS/ML

Approval Date

1982-08-31

62383 / 1

Active Ingredient

GRAMICIDIN; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

Application Number

62383

Product Number

1

Dosage Form

-

Strength

0.025MG/ML;EQ 1.75MG BASE/ML;10,000 UNITS/ML

Approval Date

1982-08-31

Regulatory Status

Discontinued

1985
18 Sep
Discontinued Application: 62617

Drug Name

NEOMYCIN SULFATE, POLYMYXIN B SULFATE & HYDROCORTISONE

Product Number

1

Dosage Form

-

Strength

1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML

Approval Date

1985-09-18

62617 / 1

Active Ingredient

HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

Application Number

62617

Product Number

1

Dosage Form

-

Strength

1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML

Approval Date

1985-09-18

Regulatory Status

Discontinued

1985
10 Jan
Discontinued Application: 62539

Drug Name

NEOMYCIN SULFATE-DEXAMETHASONE SODIUM PHOSPHATE

Product Number

1

Dosage Form

-

Strength

EQ 0.1% PHOSPHATE;EQ 3.5MG BASE/ML

Approval Date

1985-01-10

62539 / 1

Active Ingredient

DEXAMETHASONE SODIUM PHOSPHATE; NEOMYCIN SULFATE

Application Number

62539

Product Number

1

Dosage Form

-

Strength

EQ 0.1% PHOSPHATE;EQ 3.5MG BASE/ML

Approval Date

1985-01-10

Regulatory Status

Discontinued

1982
29 Sep
Discontinued Application: 62394

Drug Name

NEOMYCIN SULFATE-POLYMYXIN B SULFATE-HYDROCORTISONE

Product Number

1

Dosage Form

-

Strength

1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML

Approval Date

1982-09-29

62394 / 1

Active Ingredient

HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

Application Number

62394

Product Number

1

Dosage Form

-

Strength

1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML

Approval Date

1982-09-29

Regulatory Status

Discontinued

1985
24 Sep
Discontinued Application: 62623

Drug Name

NEOMYCIN SULFATE-POLYMYXIN B SULFATE-HYDROCORTISONE

Product Number

1

Dosage Form

-

Strength

1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML

Approval Date

1985-09-24

62623 / 1

Active Ingredient

HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

Application Number

62623

Product Number

1

Dosage Form

-

Strength

1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML

Approval Date

1985-09-24

Regulatory Status

Discontinued

1985
16 Jan
Discontinued Application: 62541

Drug Name

NYSTATIN

Product Number

1

Dosage Form

-

Strength

100,000 UNITS/ML

Approval Date

1985-01-16

62541 / 1

Active Ingredient

NYSTATIN

Application Number

62541

Product Number

1

Dosage Form

-

Strength

100,000 UNITS/ML

Approval Date

1985-01-16

Regulatory Status

Discontinued

1986
30 Jul
Discontinued Application: 62656

Drug Name

NYSTATIN AND TRIAMCINOLONE ACETONIDE

Product Number

1

Dosage Form

-

Strength

100,000 UNITS/GM;0.1%

Approval Date

1986-07-30

62656 / 1

Active Ingredient

NYSTATIN; TRIAMCINOLONE ACETONIDE

Application Number

62656

Product Number

1

Dosage Form

-

Strength

100,000 UNITS/GM;0.1%

Approval Date

1986-07-30

Regulatory Status

Discontinued

1986
30 Jul
Discontinued Application: 62657

Drug Name

NYSTATIN AND TRIAMCINOLONE ACETONIDE

Product Number

1

Dosage Form

-

Strength

100,000 UNITS/GM;0.1%

Approval Date

1986-07-30

62657 / 1

Active Ingredient

NYSTATIN; TRIAMCINOLONE ACETONIDE

Application Number

62657

Product Number

1

Dosage Form

-

Strength

100,000 UNITS/GM;0.1%

Approval Date

1986-07-30

Regulatory Status

Discontinued

1983
08 Apr
Discontinued Application: 62430

Drug Name

OCUMYCIN

Product Number

1

Dosage Form

-

Strength

500 UNITS/GM;10,000 UNITS/GM

Approval Date

1983-04-08

62430 / 1

Active Ingredient

BACITRACIN ZINC; POLYMYXIN B SULFATE

Application Number

62430

Product Number

1

Dosage Form

-

Strength

500 UNITS/GM;10,000 UNITS/GM

Approval Date

1983-04-08

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 87506

Drug Name

OPCON

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

1982-01-01

87506 / 1

Active Ingredient

NAPHAZOLINE HYDROCHLORIDE

Application Number

87506

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1989
29 Dec
Discontinued Application: 19907

Drug Name

OPTIPRANOLOL

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

1989-12-29

19907 / 1

Active Ingredient

METIPRANOLOL HYDROCHLORIDE

Application Number

19907

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

1989-12-29

Regulatory Status

Discontinued

1982
18 Nov
Discontinued Application: 62399

Drug Name

OTICAIR

Product Number

1

Dosage Form

-

Strength

1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML

Approval Date

1982-11-18

62399 / 1

Active Ingredient

HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

Application Number

62399

Product Number

1

Dosage Form

-

Strength

1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML

Approval Date

1982-11-18

Regulatory Status

Discontinued

1983
25 Feb
Discontinued Application: 88150

Drug Name

PENTOLAIR

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1983-02-25

88150 / 1

Active Ingredient

CYCLOPENTOLATE HYDROCHLORIDE

Application Number

88150

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1983-02-25

Regulatory Status

Discontinued

1987
09 Feb
Discontinued Application: 88643

Drug Name

PENTOLAIR

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

1987-02-09

88643 / 1

Active Ingredient

CYCLOPENTOLATE HYDROCHLORIDE

Application Number

88643

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

1987-02-09

Regulatory Status

Discontinued

1984
29 Feb
Discontinued Application: 88415

Drug Name

PREDAIR

Product Number

1

Dosage Form

-

Strength

EQ 0.11% PHOSPHATE

Approval Date

1984-02-29

88415 / 1

Active Ingredient

PREDNISOLONE SODIUM PHOSPHATE

Application Number

88415

Product Number

1

Dosage Form

-

Strength

EQ 0.11% PHOSPHATE

Approval Date

1984-02-29

Regulatory Status

Discontinued

1983
28 Mar
Discontinued Application: 88165

Drug Name

PREDAIR FORTE

Product Number

1

Dosage Form

-

Strength

EQ 0.9% PHOSPHATE

Approval Date

1983-03-28

88165 / 1

Active Ingredient

PREDNISOLONE SODIUM PHOSPHATE

Application Number

88165

Product Number

1

Dosage Form

-

Strength

EQ 0.9% PHOSPHATE

Approval Date

1983-03-28

Regulatory Status

Discontinued

1994
29 Jul
Discontinued Application: 40065

Drug Name

PREDNISOLONE SODIUM PHOSPHATE

Product Number

1

Dosage Form

-

Strength

EQ 0.11% PHOSPHATE

Approval Date

1994-07-29

40065 / 1

Active Ingredient

PREDNISOLONE SODIUM PHOSPHATE

Application Number

40065

Product Number

1

Dosage Form

-

Strength

EQ 0.11% PHOSPHATE

Approval Date

1994-07-29

Regulatory Status

Discontinued

1983
19 Apr
Discontinued Application: 88007

Drug Name

PREDSULFAIR

Product Number

1

Dosage Form

-

Strength

0.5%;10%

Approval Date

1983-04-19

88007 / 1

Active Ingredient

PREDNISOLONE ACETATE; SULFACETAMIDE SODIUM

Application Number

88007

Product Number

1

Dosage Form

-

Strength

0.5%;10%

Approval Date

1983-04-19

Regulatory Status

Discontinued

1983
15 Apr
Discontinued Application: 88032

Drug Name

PREDSULFAIR

Product Number

1

Dosage Form

-

Strength

0.5%;10%

Approval Date

1983-04-15

88032 / 1

Active Ingredient

PREDNISOLONE ACETATE; SULFACETAMIDE SODIUM

Application Number

88032

Product Number

1

Dosage Form

-

Strength

0.5%;10%

Approval Date

1983-04-15

Regulatory Status

Discontinued

1985
24 Dec
Discontinued Application: 88837

Drug Name

PREDSULFAIR II

Product Number

1

Dosage Form

-

Strength

0.2%;10%

Approval Date

1985-12-24

88837 / 1

Active Ingredient

PREDNISOLONE ACETATE; SULFACETAMIDE SODIUM

Application Number

88837

Product Number

1

Dosage Form

-

Strength

0.2%;10%

Approval Date

1985-12-24

Regulatory Status

Discontinued

1985
20 Nov
Discontinued Application: 88824

Drug Name

PROCAINAMIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

100MG/ML

Approval Date

1985-11-20

88824 / 1

Active Ingredient

PROCAINAMIDE HYDROCHLORIDE

Application Number

88824

Product Number

1

Dosage Form

-

Strength

100MG/ML

Approval Date

1985-11-20

Regulatory Status

Discontinued

1985
20 Nov
Discontinued Application: 88830

Drug Name

PROCAINAMIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

500MG/ML

Approval Date

1985-11-20

88830 / 1

Active Ingredient

PROCAINAMIDE HYDROCHLORIDE

Application Number

88830

Product Number

1

Dosage Form

-

Strength

500MG/ML

Approval Date

1985-11-20

Regulatory Status

Discontinued

2005
08 Apr
Discontinued Application: 21737

Drug Name

RETISERT

Product Number

1

Dosage Form

-

Strength

0.59MG

Approval Date

2005-04-08

21737 / 1

Active Ingredient

FLUOCINOLONE ACETONIDE

Application Number

21737

Product Number

1

Dosage Form

-

Strength

0.59MG

Approval Date

2005-04-08

Regulatory Status

Discontinued

1985
17 May
Discontinued Application: 88947

Drug Name

SULFACETAMIDE SODIUM

Product Number

1

Dosage Form

-

Strength

10%

Approval Date

1985-05-17

88947 / 1

Active Ingredient

SULFACETAMIDE SODIUM

Application Number

88947

Product Number

1

Dosage Form

-

Strength

10%

Approval Date

1985-05-17

Regulatory Status

Discontinued

1982
13 Dec
Discontinued Application: 87949

Drug Name

SULFAIR 10

Product Number

1

Dosage Form

-

Strength

10%

Approval Date

1982-12-13

87949 / 1

Active Ingredient

SULFACETAMIDE SODIUM

Application Number

87949

Product Number

1

Dosage Form

-

Strength

10%

Approval Date

1982-12-13

Regulatory Status

Discontinued

1982
22 Dec
Discontinued Application: 88000

Drug Name

SULFAIR 10

Product Number

1

Dosage Form

-

Strength

10%

Approval Date

1982-12-22

88000 / 1

Active Ingredient

SULFACETAMIDE SODIUM

Application Number

88000

Product Number

1

Dosage Form

-

Strength

10%

Approval Date

1982-12-22

Regulatory Status

Discontinued

1983
13 Oct
Discontinued Application: 88385

Drug Name

SULFAIR FORTE

Product Number

1

Dosage Form

-

Strength

30%

Approval Date

1983-10-13

88385 / 1

Active Ingredient

SULFACETAMIDE SODIUM

Application Number

88385

Product Number

1

Dosage Form

-

Strength

30%

Approval Date

1983-10-13

Regulatory Status

Discontinued

1983
25 May
Discontinued Application: 88186

Drug Name

SULFAIR-15

Product Number

1

Dosage Form

-

Strength

15%

Approval Date

1983-05-25

88186 / 1

Active Ingredient

SULFACETAMIDE SODIUM

Application Number

88186

Product Number

1

Dosage Form

-

Strength

15%

Approval Date

1983-05-25

Regulatory Status

Discontinued

1982
28 Dec
Discontinued Application: 88089

Drug Name

SULPHRIN

Product Number

1

Dosage Form

-

Strength

0.5%;10%

Approval Date

1982-12-28

88089 / 1

Active Ingredient

PREDNISOLONE ACETATE; SULFACETAMIDE SODIUM

Application Number

88089

Product Number

1

Dosage Form

-

Strength

0.5%;10%

Approval Date

1982-12-28

Regulatory Status

Discontinued

1983
03 Feb
Discontinued Application: 87818

Drug Name

SULTEN-10

Product Number

1

Dosage Form

-

Strength

10%

Approval Date

1983-02-03

87818 / 1

Active Ingredient

SULFACETAMIDE SODIUM

Application Number

87818

Product Number

1

Dosage Form

-

Strength

10%

Approval Date

1983-02-03

Regulatory Status

Discontinued

1997
25 Mar
Discontinued Application: 74776

Drug Name

TIMOLOL MALEATE

Product Number

1

Dosage Form

-

Strength

EQ 0.5% BASE

Approval Date

1997-03-25

74776 / 1

Active Ingredient

TIMOLOL MALEATE

Application Number

74776

Product Number

1

Dosage Form

-

Strength

EQ 0.5% BASE

Approval Date

1997-03-25

Regulatory Status

Discontinued

1997
25 Mar
Discontinued Application: 74778

Drug Name

TIMOLOL MALEATE

Product Number

1

Dosage Form

-

Strength

EQ 0.25% BASE

Approval Date

1997-03-25

74778 / 1

Active Ingredient

TIMOLOL MALEATE

Application Number

74778

Product Number

1

Dosage Form

-

Strength

EQ 0.25% BASE

Approval Date

1997-03-25

Regulatory Status

Discontinued

1982
10 Aug
Discontinued Application: 87912

Drug Name

TRIAMCINOLONE ACETONIDE

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

1982-08-10

87912 / 1

Active Ingredient

TRIAMCINOLONE ACETONIDE

Application Number

87912

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

1982-08-10

Regulatory Status

Discontinued

1982
10 Aug
Discontinued Application: 87921

Drug Name

TRIAMCINOLONE ACETONIDE

Product Number

1

Dosage Form

-

Strength

0.025%

Approval Date

1982-08-10

87921 / 1

Active Ingredient

TRIAMCINOLONE ACETONIDE

Application Number

87921

Product Number

1

Dosage Form

-

Strength

0.025%

Approval Date

1982-08-10

Regulatory Status

Discontinued

1982
10 Aug
Discontinued Application: 87922

Drug Name

TRIAMCINOLONE ACETONIDE

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

1982-08-10

87922 / 1

Active Ingredient

TRIAMCINOLONE ACETONIDE

Application Number

87922

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

1982-08-10

Regulatory Status

Discontinued

1996
04 Mar
Discontinued Application: 20569

Drug Name

VITRASERT

Product Number

1

Dosage Form

-

Strength

4.5MG

Approval Date

1996-03-04

20569 / 1

Active Ingredient

GANCICLOVIR

Application Number

20569

Product Number

1

Dosage Form

-

Strength

4.5MG

Approval Date

1996-03-04

Regulatory Status

Discontinued

1982
02 Jul
Discontinued Application: 62389

Drug Name

ZINC BACITRACIN,NEOMYCIN SULFATE,POLYMYXIN B SULFATE & HYDROCORTISONE

Product Number

1

Dosage Form

-

Strength

400 UNITS/GM;1%;EQ 3.5MG BASE/GM;10,000 UNITS/GM

Approval Date

1982-07-02

62389 / 1

Active Ingredient

BACITRACIN ZINC; HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

Application Number

62389

Product Number

1

Dosage Form

-

Strength

400 UNITS/GM;1%;EQ 3.5MG BASE/GM;10,000 UNITS/GM

Approval Date

1982-07-02

Regulatory Status

Discontinued

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Drug Status Breakdown
87 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

ACETIC ACID 2% IN AQUEOUS ALUMINUM ACETATE

Application Number

40063

Product Number

1

Active Ingredient

ACETIC ACID, GLACIAL; ALUMINUM ACETATE

Dosage Form

-

Strength

2%;0.79%

FDA Approved Drug Data

Approved drug product information

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