Thea Pharma RX
FDA Approved Drugs

Thea Pharma 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 8
  • Latest Approval Date Sep 09, 2025
  • Data Source FDA
  • First Approval Date Mar 31, 1995
All
10
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Discontinued
2
View
RX
8
View
Company Overview

Company

Thea Pharma RX

Country

U.S.A

Website

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Company Snapshot

Thea Pharma RX

420 Bedford Street, Suite 150 Lexington, MA 02420

U.S.A

theapharmainc.com/ View on Map
FDA Approved Drug Records ( 8 records )
2008
07 Oct
RX Application: 22221

Drug Name

AKTEN

Product Number

1

Dosage Form

-

Strength

3.5%

Approval Date

2008-10-07

22221 / 1

Active Ingredient

LIDOCAINE HYDROCHLORIDE

Application Number

22221

Product Number

1

Dosage Form

-

Strength

3.5%

Approval Date

2008-10-07

Regulatory Status

RX

2007
27 Apr
RX Application: 50810

Drug Name

AZASITE

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

2007-04-27

50810 / 1

Active Ingredient

AZITHROMYCIN

Application Number

50810

Product Number

1

Dosage Form

-

Strength

1%

Approval Date

2007-04-27

Regulatory Status

RX

1995
31 Mar
RX Application: 20439

Drug Name

BETIMOL

Product Number

2

Dosage Form

-

Strength

0.5%

Approval Date

1995-03-31

20439 / 2

Active Ingredient

TIMOLOL

Application Number

20439

Product Number

2

Dosage Form

-

Strength

0.5%

Approval Date

1995-03-31

Regulatory Status

RX

1998
07 Apr
RX Application: 20869

Drug Name

COSOPT

Product Number

1

Dosage Form

-

Strength

EQ 2% BASE;EQ 0.5% BASE

Approval Date

1998-04-07

20869 / 1

Active Ingredient

DORZOLAMIDE HYDROCHLORIDE; TIMOLOL MALEATE

Application Number

20869

Product Number

1

Dosage Form

-

Strength

EQ 2% BASE;EQ 0.5% BASE

Approval Date

1998-04-07

Regulatory Status

RX

2012
01 Feb
RX Application: 202667

Drug Name

COSOPT PF

Product Number

1

Dosage Form

-

Strength

EQ 2% BASE;EQ 0.5% BASE

Approval Date

2012-02-01

202667 / 1

Active Ingredient

DORZOLAMIDE HYDROCHLORIDE; TIMOLOL MALEATE

Application Number

202667

Product Number

1

Dosage Form

-

Strength

EQ 2% BASE;EQ 0.5% BASE

Approval Date

2012-02-01

Regulatory Status

RX

2022
13 Dec
RX Application: 216472

Drug Name

IYUZEH

Product Number

1

Dosage Form

-

Strength

0.005%

Approval Date

2022-12-13

216472 / 1

Active Ingredient

LATANOPROST

Application Number

216472

Product Number

1

Dosage Form

-

Strength

0.005%

Approval Date

2022-12-13

Regulatory Status

RX

2012
10 Feb
RX Application: 202514

Drug Name

ZIOPTAN

Product Number

1

Dosage Form

-

Strength

0.0015%

Approval Date

2012-02-10

202514 / 1

Active Ingredient

TAFLUPROST

Application Number

202514

Product Number

1

Dosage Form

-

Strength

0.0015%

Approval Date

2012-02-10

Regulatory Status

RX

2025
09 Sep
RX Application: 217307

Drug Name

ZOLYMBUS

Product Number

1

Dosage Form

-

Strength

0.01%

Approval Date

2025-09-09

217307 / 1

Active Ingredient

BIMATOPROST

Application Number

217307

Product Number

1

Dosage Form

-

Strength

0.01%

Approval Date

2025-09-09

Regulatory Status

RX

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Drug Status Breakdown
8 total
  • RX
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

AKTEN

Application Number

22221

Product Number

1

Active Ingredient

LIDOCAINE HYDROCHLORIDE

Dosage Form

-

Strength

3.5%

FDA Approved Drug Data

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