Bausch & Lomb Incorporated OTC
FDA Approved Drugs

Bausch & Lomb Incorporated 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 4
  • Latest Approval Date Feb 11, 2015
  • Data Source FDA
  • First Approval Date Jun 08, 1994
All
114
View
Unclassified
2
View
Discontinued
87
View
OTC
4
View
RX
21
View
Company Overview

Company

Bausch & Lomb Incorporated OTC

Country

Canada

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Company Snapshot

Bausch & Lomb Incorporated OTC

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

Canada

www.bausch.com/ View on Map
FDA Approved Drug Records ( 4 records )
2006
01 Dec
OTC Application: 21996

Drug Name

ALAWAY

Product Number

1

Dosage Form

-

Strength

EQ 0.025% BASE

Approval Date

2006-12-01

21996 / 1

Active Ingredient

KETOTIFEN FUMARATE

Application Number

21996

Product Number

1

Dosage Form

-

Strength

EQ 0.025% BASE

Approval Date

2006-12-01

Regulatory Status

OTC

2015
11 Feb
OTC Application: 21996

Drug Name

CHILDRENS ALAWAY

Product Number

2

Dosage Form

-

Strength

EQ 0.025% BASE

Approval Date

2015-02-11

21996 / 2

Active Ingredient

KETOTIFEN FUMARATE

Application Number

21996

Product Number

2

Dosage Form

-

Strength

EQ 0.025% BASE

Approval Date

2015-02-11

Regulatory Status

OTC

2001
03 Jul
OTC Application: 75702

Drug Name

CROMOLYN SODIUM

Product Number

1

Dosage Form

-

Strength

5.2MG/SPRAY

Approval Date

2001-07-03

75702 / 1

Active Ingredient

CROMOLYN SODIUM

Application Number

75702

Product Number

1

Dosage Form

-

Strength

5.2MG/SPRAY

Approval Date

2001-07-03

Regulatory Status

OTC

1994
08 Jun
OTC Application: 20065

Drug Name

OPCON-A

Product Number

1

Dosage Form

-

Strength

0.02675%;0.315%

Approval Date

1994-06-08

20065 / 1

Active Ingredient

NAPHAZOLINE HYDROCHLORIDE; PHENIRAMINE MALEATE

Application Number

20065

Product Number

1

Dosage Form

-

Strength

0.02675%;0.315%

Approval Date

1994-06-08

Regulatory Status

OTC

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Drug Status Breakdown
4 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

ALAWAY

Application Number

21996

Product Number

1

Active Ingredient

KETOTIFEN FUMARATE

Dosage Form

-

Strength

EQ 0.025% BASE

FDA Approved Drug Data

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