Alcon Inc OTC
FDA Approved Drugs

Alcon Inc 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 5
  • Latest Approval Date Jan 30, 2015
  • Data Source FDA
  • First Approval Date Jun 08, 1994
All
60
View
Unclassified
1
View
Discontinued
34
View
OTC
5
View
RX
20
View
Company Overview

Company

Alcon Inc OTC

Country

U.S.A

Website

Visit Website

Email

alcon@alconpharma.com

Social Profiles

LinkedIn
Company Snapshot

Alcon Inc OTC

6201 South Freeway Mail Code AB2-6 Fort Worth, TX 76134-2001

U.S.A

www.alcon.com/ alcon@alconpharma.com View on Map
FDA Approved Drug Records ( 5 records )
1994
08 Jun
OTC Application: 20226

Drug Name

NAPHCON-A

Product Number

1

Dosage Form

-

Strength

0.025%;0.3%

Approval Date

1994-06-08

20226 / 1

Active Ingredient

NAPHAZOLINE HYDROCHLORIDE; PHENIRAMINE MALEATE

Application Number

20226

Product Number

1

Dosage Form

-

Strength

0.025%;0.3%

Approval Date

1994-06-08

Regulatory Status

OTC

2004
22 Dec
OTC Application: 21545

Drug Name

PATADAY ONCE DAILY RELIEF

Product Number

1

Dosage Form

-

Strength

EQ 0.2% BASE

Approval Date

2004-12-22

21545 / 1

Active Ingredient

OLOPATADINE HYDROCHLORIDE

Application Number

21545

Product Number

1

Dosage Form

-

Strength

EQ 0.2% BASE

Approval Date

2004-12-22

Regulatory Status

OTC

2015
30 Jan
OTC Application: 206276

Drug Name

PATADAY ONCE DAILY RELIEF

Product Number

1

Dosage Form

-

Strength

EQ 0.7% BASE

Approval Date

2015-01-30

206276 / 1

Active Ingredient

OLOPATADINE HYDROCHLORIDE

Application Number

206276

Product Number

1

Dosage Form

-

Strength

EQ 0.7% BASE

Approval Date

2015-01-30

Regulatory Status

OTC

1996
18 Dec
OTC Application: 20688

Drug Name

PATADAY TWICE DAILY RELIEF

Product Number

1

Dosage Form

-

Strength

EQ 0.1% BASE

Approval Date

1996-12-18

20688 / 1

Active Ingredient

OLOPATADINE HYDROCHLORIDE

Application Number

20688

Product Number

1

Dosage Form

-

Strength

EQ 0.1% BASE

Approval Date

1996-12-18

Regulatory Status

OTC

2008
02 Sep
OTC Application: 77200

Drug Name

ZADITOR

Product Number

1

Dosage Form

-

Strength

EQ 0.025% BASE

Approval Date

2008-09-02

77200 / 1

Active Ingredient

KETOTIFEN FUMARATE

Application Number

77200

Product Number

1

Dosage Form

-

Strength

EQ 0.025% BASE

Approval Date

2008-09-02

Regulatory Status

OTC

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Drug Status Breakdown
5 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

NAPHCON-A

Application Number

20226

Product Number

1

Active Ingredient

NAPHAZOLINE HYDROCHLORIDE; PHENIRAMINE MALEATE

Dosage Form

-

Strength

0.025%;0.3%

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

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