Bausch & Lomb Incorporated RX
FDA Approved Drugs

Bausch & Lomb Incorporated RX

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.

RX
  • Total Records 21
  • Latest Approval Date Aug 18, 2021
  • Data Source FDA
  • First Approval Date Sep 22, 1993
All
114
View
Unclassified
2
View
Discontinued
87
View
OTC
4
View
RX
21
View
Company Overview

Company

Bausch & Lomb Incorporated RX

Country

Canada

Website

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Company Snapshot

Bausch & Lomb Incorporated RX

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

Canada

www.bausch.com/ View on Map
FDA Approved Drug Records ( 21 records )
1998
09 Mar
RX Application: 20803

Drug Name

ALREX

Product Number

1

Dosage Form

-

Strength

0.2%

Approval Date

1998-03-09

20803 / 1

Active Ingredient

LOTEPREDNOL ETABONATE

Application Number

20803

Product Number

1

Dosage Form

-

Strength

0.2%

Approval Date

1998-03-09

Regulatory Status

RX

2009
28 May
RX Application: 22308

Drug Name

BESIVANCE

Product Number

1

Dosage Form

-

Strength

EQ 0.6% BASE

Approval Date

2009-05-28

22308 / 1

Active Ingredient

BESIFLOXACIN HYDROCHLORIDE

Application Number

22308

Product Number

1

Dosage Form

-

Strength

EQ 0.6% BASE

Approval Date

2009-05-28

Regulatory Status

RX

2021
18 Aug
RX Application: 204884

Drug Name

BRINZOLAMIDE

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

2021-08-18

204884 / 1

Active Ingredient

BRINZOLAMIDE

Application Number

204884

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

2021-08-18

Regulatory Status

RX

2007
28 Dec
RX Application: 78792

Drug Name

DICLOFENAC SODIUM

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

2007-12-28

78792 / 1

Active Ingredient

DICLOFENAC SODIUM

Application Number

78792

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

2007-12-28

Regulatory Status

RX

2009
25 Jun
RX Application: 90143

Drug Name

DORZOLAMIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 2% BASE

Approval Date

2009-06-25

90143 / 1

Active Ingredient

DORZOLAMIDE HYDROCHLORIDE

Application Number

90143

Product Number

1

Dosage Form

-

Strength

EQ 2% BASE

Approval Date

2009-06-25

Regulatory Status

RX

2009
14 Jul
RX Application: 90037

Drug Name

DORZOLAMIDE HYDROCHLORIDE AND TIMOLOL MALEATE

Product Number

1

Dosage Form

-

Strength

EQ 2% BASE;EQ 0.5% BASE

Approval Date

2009-07-14

90037 / 1

Active Ingredient

DORZOLAMIDE HYDROCHLORIDE; TIMOLOL MALEATE

Application Number

90037

Product Number

1

Dosage Form

-

Strength

EQ 2% BASE;EQ 0.5% BASE

Approval Date

2009-07-14

Regulatory Status

RX

1995
04 Jan
RX Application: 74447

Drug Name

FLURBIPROFEN SODIUM

Product Number

1

Dosage Form

-

Strength

0.03%

Approval Date

1995-01-04

74447 / 1

Active Ingredient

FLURBIPROFEN SODIUM

Application Number

74447

Product Number

1

Dosage Form

-

Strength

0.03%

Approval Date

1995-01-04

Regulatory Status

RX

2004
04 Jun
RX Application: 21516

Drug Name

ISTALOL

Product Number

1

Dosage Form

-

Strength

EQ 0.5% BASE

Approval Date

2004-06-04

21516 / 1

Active Ingredient

TIMOLOL MALEATE

Application Number

21516

Product Number

1

Dosage Form

-

Strength

EQ 0.5% BASE

Approval Date

2004-06-04

Regulatory Status

RX

2011
22 Mar
RX Application: 201006

Drug Name

LATANOPROST

Product Number

1

Dosage Form

-

Strength

0.005%

Approval Date

2011-03-22

201006 / 1

Active Ingredient

LATANOPROST

Application Number

201006

Product Number

1

Dosage Form

-

Strength

0.005%

Approval Date

2011-03-22

Regulatory Status

RX

1998
09 Mar
RX Application: 20583

Drug Name

LOTEMAX

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

1998-03-09

20583 / 1

Active Ingredient

LOTEPREDNOL ETABONATE

Application Number

20583

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

1998-03-09

Regulatory Status

RX

2011
15 Apr
RX Application: 200738

Drug Name

LOTEMAX

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

2011-04-15

200738 / 1

Active Ingredient

LOTEPREDNOL ETABONATE

Application Number

200738

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

2011-04-15

Regulatory Status

RX

1993
22 Sep
RX Application: 20213

Drug Name

MIOCHOL-E

Product Number

1

Dosage Form

-

Strength

20MG/VIAL

Approval Date

1993-09-22

20213 / 1

Active Ingredient

ACETYLCHOLINE CHLORIDE

Application Number

20213

Product Number

1

Dosage Form

-

Strength

20MG/VIAL

Approval Date

1993-09-22

Regulatory Status

RX

2004
14 May
RX Application: 76622

Drug Name

OFLOXACIN

Product Number

1

Dosage Form

-

Strength

0.3%

Approval Date

2004-05-14

76622 / 1

Active Ingredient

OFLOXACIN

Application Number

76622

Product Number

1

Dosage Form

-

Strength

0.3%

Approval Date

2004-05-14

Regulatory Status

RX

2013
05 Apr
RX Application: 203168

Drug Name

PROLENSA

Product Number

1

Dosage Form

-

Strength

EQ 0.07% ACID

Approval Date

2013-04-05

203168 / 1

Active Ingredient

BROMFENAC SODIUM

Application Number

203168

Product Number

1

Dosage Form

-

Strength

EQ 0.07% ACID

Approval Date

2013-04-05

Regulatory Status

RX

1994
28 Dec
RX Application: 40066

Drug Name

SULFACETAMIDE SODIUM

Product Number

1

Dosage Form

-

Strength

10%

Approval Date

1994-12-28

40066 / 1

Active Ingredient

SULFACETAMIDE SODIUM

Application Number

40066

Product Number

1

Dosage Form

-

Strength

10%

Approval Date

1994-12-28

Regulatory Status

RX

1995
29 Dec
RX Application: 74449

Drug Name

SULFACETAMIDE SODIUM AND PREDNISOLONE SODIUM PHOSPHATE

Product Number

1

Dosage Form

-

Strength

EQ 0.23% PHOSPHATE;10%

Approval Date

1995-12-29

74449 / 1

Active Ingredient

PREDNISOLONE SODIUM PHOSPHATE; SULFACETAMIDE SODIUM

Application Number

74449

Product Number

1

Dosage Form

-

Strength

EQ 0.23% PHOSPHATE;10%

Approval Date

1995-12-29

Regulatory Status

RX

1994
27 Jul
RX Application: 40064

Drug Name

TROPICAMIDE

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1994-07-27

40064 / 1

Active Ingredient

TROPICAMIDE

Application Number

40064

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1994-07-27

Regulatory Status

RX

1994
27 Jul
RX Application: 40067

Drug Name

TROPICAMIDE

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

1994-07-27

40067 / 1

Active Ingredient

TROPICAMIDE

Application Number

40067

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

1994-07-27

Regulatory Status

RX

2017
02 Nov
RX Application: 207795

Drug Name

VYZULTA

Product Number

1

Dosage Form

-

Strength

0.024%

Approval Date

2017-11-02

207795 / 1

Active Ingredient

LATANOPROSTENE BUNOD

Application Number

207795

Product Number

1

Dosage Form

-

Strength

0.024%

Approval Date

2017-11-02

Regulatory Status

RX

2009
15 Sep
RX Application: 22211

Drug Name

ZIRGAN

Product Number

1

Dosage Form

-

Strength

0.15%

Approval Date

2009-09-15

22211 / 1

Active Ingredient

GANCICLOVIR

Application Number

22211

Product Number

1

Dosage Form

-

Strength

0.15%

Approval Date

2009-09-15

Regulatory Status

RX

2004
14 Dec
RX Application: 50804

Drug Name

ZYLET

Product Number

1

Dosage Form

-

Strength

0.5%;0.3%

Approval Date

2004-12-14

50804 / 1

Active Ingredient

LOTEPREDNOL ETABONATE; TOBRAMYCIN

Application Number

50804

Product Number

1

Dosage Form

-

Strength

0.5%;0.3%

Approval Date

2004-12-14

Regulatory Status

RX

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Drug Status Breakdown
21 total
  • RX
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

ALREX

Application Number

20803

Product Number

1

Active Ingredient

LOTEPREDNOL ETABONATE

Dosage Form

-

Strength

0.2%

FDA Approved Drug Data

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