Alcon Inc RX
FDA Approved Drugs

Alcon Inc 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 20
  • Latest Approval Date May 28, 2025
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
60
View
Unclassified
1
View
Discontinued
34
View
OTC
5
View
RX
20
View
Company Overview

Company

Alcon Inc RX

Country

U.S.A

Website

Visit Website

Email

alcon@alconpharma.com

Social Profiles

LinkedIn
Company Snapshot

Alcon Inc RX

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 ( 20 records )
1982
01 Jan
RX Application: 80027

Drug Name

ALCAINE

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

1982-01-01

80027 / 1

Active Ingredient

PROPARACAINE HYDROCHLORIDE

Application Number

80027

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

1982-01-01

Regulatory Status

RX

1986
17 Dec
RX Application: 18634

Drug Name

BETADINE

Product Number

1

Dosage Form

-

Strength

5%

Approval Date

1986-12-17

18634 / 1

Active Ingredient

POVIDONE-IODINE

Application Number

18634

Product Number

1

Dosage Form

-

Strength

5%

Approval Date

1986-12-17

Regulatory Status

RX

1997
10 Dec
RX Application: 20742

Drug Name

BSS

Product Number

1

Dosage Form

-

Strength

0.48MG/ML;0.3MG/ML;0.75MG/ML;3.9MG/ML;6.4MG/ML;1.7MG/ML

Approval Date

1997-12-10

20742 / 1

Active Ingredient

CALCIUM CHLORIDE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM CITRATE

Application Number

20742

Product Number

1

Dosage Form

-

Strength

0.48MG/ML;0.3MG/ML;0.75MG/ML;3.9MG/ML;6.4MG/ML;1.7MG/ML

Approval Date

1997-12-10

Regulatory Status

RX

1982
01 Jan
RX Application: 18469

Drug Name

BSS PLUS

Product Number

1

Dosage Form

-

Strength

0.154MG/ML;0.92MG/ML;0.184MG/ML;0.2MG/ML;0.38MG/ML;2.1MG/ML;7.14MG/ML;0.42MG/ML

Approval Date

1982-01-01

18469 / 1

Active Ingredient

CALCIUM CHLORIDE; DEXTROSE; GLUTATHIONE DISULFIDE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM PHOSPHATE

Application Number

18469

Product Number

1

Dosage Form

-

Strength

0.154MG/ML;0.92MG/ML;0.184MG/ML;0.2MG/ML;0.38MG/ML;2.1MG/ML;7.14MG/ML;0.42MG/ML

Approval Date

1982-01-01

Regulatory Status

RX

1982
01 Jan
RX Application: 84108

Drug Name

CYCLOGYL

Product Number

1

Dosage Form

-

Strength

2%

Approval Date

1982-01-01

84108 / 1

Active Ingredient

CYCLOPENTOLATE HYDROCHLORIDE

Application Number

84108

Product Number

1

Dosage Form

-

Strength

2%

Approval Date

1982-01-01

Regulatory Status

RX

1982
01 Jan
RX Application: 84109

Drug Name

CYCLOGYL

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

1982-01-01

84109 / 1

Active Ingredient

CYCLOPENTOLATE HYDROCHLORIDE

Application Number

84109

Product Number

1

Dosage Form

-

Strength

0.5%

Approval Date

1982-01-01

Regulatory Status

RX

1982
01 Jan
RX Application: 84110

Drug Name

CYCLOGYL

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

84110 / 1

Active Ingredient

CYCLOPENTOLATE HYDROCHLORIDE

Application Number

84110

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

Regulatory Status

RX

1982
01 Jan
RX Application: 84300

Drug Name

CYCLOMYDRIL

Product Number

1

Dosage Form

-

Strength

0.2%;1%

Approval Date

1982-01-01

84300 / 1

Active Ingredient

CYCLOPENTOLATE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE

Application Number

84300

Product Number

1

Dosage Form

-

Strength

0.2%;1%

Approval Date

1982-01-01

Regulatory Status

RX

2020
26 Oct
RX Application: 210933

Drug Name

EYSUVIS

Product Number

1

Dosage Form

-

Strength

0.25%

Approval Date

2020-10-26

210933 / 1

Active Ingredient

LOTEPREDNOL ETABONATE

Application Number

210933

Product Number

1

Dosage Form

-

Strength

0.25%

Approval Date

2020-10-26

Regulatory Status

RX

2006
28 Mar
RX Application: 21980

Drug Name

FLUORESCITE

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/5ML (EQ 100MG BASE/ML)

Approval Date

2006-03-28

21980 / 1

Active Ingredient

FLUORESCEIN SODIUM

Application Number

21980

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/5ML (EQ 100MG BASE/ML)

Approval Date

2006-03-28

Regulatory Status

RX

2018
22 Aug
RX Application: 210565

Drug Name

INVELTYS

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

2018-08-22

210565 / 1

Active Ingredient

LOTEPREDNOL ETABONATE

Application Number

210565

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

2018-08-22

Regulatory Status

RX

2016
01 Dec
RX Application: 208151

Drug Name

ISOPTO ATROPINE

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

2016-12-01

208151 / 1

Active Ingredient

ATROPINE SULFATE

Application Number

208151

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

2016-12-01

Regulatory Status

RX

1982
01 Jan
RX Application: 16968

Drug Name

MIOSTAT

Product Number

1

Dosage Form

-

Strength

0.01%

Approval Date

1982-01-01

16968 / 1

Active Ingredient

CARBACHOL

Application Number

16968

Product Number

1

Dosage Form

-

Strength

0.01%

Approval Date

1982-01-01

Regulatory Status

RX

1982
01 Jan
RX Application: 84306

Drug Name

MYDRIACYL

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

84306 / 1

Active Ingredient

TROPICAMIDE

Application Number

84306

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

1982-01-01

Regulatory Status

RX

2015
15 Jan
RX Application: 207926

Drug Name

PHENYLEPHRINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

2.5%

Approval Date

2015-01-15

207926 / 1

Active Ingredient

PHENYLEPHRINE HYDROCHLORIDE

Application Number

207926

Product Number

1

Dosage Form

-

Strength

2.5%

Approval Date

2015-01-15

Regulatory Status

RX

2015
15 Jan
RX Application: 207926

Drug Name

PHENYLEPHRINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

10%

Approval Date

2015-01-15

207926 / 2

Active Ingredient

PHENYLEPHRINE HYDROCHLORIDE

Application Number

207926

Product Number

2

Dosage Form

-

Strength

10%

Approval Date

2015-01-15

Regulatory Status

RX

2017
18 Dec
RX Application: 208254

Drug Name

RHOPRESSA

Product Number

1

Dosage Form

-

Strength

EQ 0.02% BASE

Approval Date

2017-12-18

208254 / 1

Active Ingredient

NETARSUDIL MESYLATE

Application Number

208254

Product Number

1

Dosage Form

-

Strength

EQ 0.02% BASE

Approval Date

2017-12-18

Regulatory Status

RX

2019
12 Mar
RX Application: 208259

Drug Name

ROCKLATAN

Product Number

1

Dosage Form

-

Strength

0.005%;EQ 0.02% BASE

Approval Date

2019-03-12

208259 / 1

Active Ingredient

LATANOPROST; NETARSUDIL DIMESYLATE

Application Number

208259

Product Number

1

Dosage Form

-

Strength

0.005%;EQ 0.02% BASE

Approval Date

2019-03-12

Regulatory Status

RX

2013
19 Apr
RX Application: 204251

Drug Name

SIMBRINZA

Product Number

1

Dosage Form

-

Strength

0.2%;1%

Approval Date

2013-04-19

204251 / 1

Active Ingredient

BRIMONIDINE TARTRATE; BRINZOLAMIDE

Application Number

204251

Product Number

1

Dosage Form

-

Strength

0.2%;1%

Approval Date

2013-04-19

Regulatory Status

RX

2025
28 May
RX Application: 217370

Drug Name

TRYPTYR

Product Number

1

Dosage Form

-

Strength

0.003%

Approval Date

2025-05-28

217370 / 1

Active Ingredient

ACOLTREMON

Application Number

217370

Product Number

1

Dosage Form

-

Strength

0.003%

Approval Date

2025-05-28

Regulatory Status

RX

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Drug Status Breakdown
20 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

ALCAINE

Application Number

80027

Product Number

1

Active Ingredient

PROPARACAINE HYDROCHLORIDE

Dosage Form

-

Strength

0.5%

FDA Approved Drug Data

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