Icon Plc
FDA Approved Drugs

Icon Plc

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.

Discontinued
  • Total Records 15
  • Latest Approval Date Mar 04, 1986
  • Data Source FDA
  • First Approval Date Jan 01, 1982
Company Overview

Company

Icon Plc

Country

Ireland

Website

Visit Website

Email

Social Profiles

LinkedIn X / Twitter
Company Snapshot

Icon Plc

South County Business Park Leopardstown Dublin 18

Ireland

www.iconplc.com/ View on Map
FDA Approved Drug Records ( 15 records )
1982
01 Jan
Discontinued Application: 11771

Drug Name

ATHROMBIN

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

11771 / 1

Active Ingredient

WARFARIN SODIUM

Application Number

11771

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 11771

Drug Name

ATHROMBIN

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

11771 / 2

Active Ingredient

WARFARIN SODIUM

Application Number

11771

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 11771

Drug Name

ATHROMBIN

Product Number

3

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

11771 / 3

Active Ingredient

WARFARIN SODIUM

Application Number

11771

Product Number

3

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 11771

Drug Name

ATHROMBIN-K

Product Number

4

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

11771 / 4

Active Ingredient

WARFARIN POTASSIUM

Application Number

11771

Product Number

4

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 11771

Drug Name

ATHROMBIN-K

Product Number

5

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

11771 / 5

Active Ingredient

WARFARIN POTASSIUM

Application Number

11771

Product Number

5

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 11771

Drug Name

ATHROMBIN-K

Product Number

6

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

11771 / 6

Active Ingredient

WARFARIN POTASSIUM

Application Number

11771

Product Number

6

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 11771

Drug Name

ATHROMBIN-K

Product Number

7

Dosage Form

-

Strength

2MG

Approval Date

1982-01-01

11771 / 7

Active Ingredient

WARFARIN POTASSIUM

Application Number

11771

Product Number

7

Dosage Form

-

Strength

2MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 11642

Drug Name

CARDIOQUIN

Product Number

2

Dosage Form

-

Strength

275MG

Approval Date

1982-01-01

11642 / 2

Active Ingredient

QUINIDINE POLYGALACTURONATE

Application Number

11642

Product Number

2

Dosage Form

-

Strength

275MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 11340

Drug Name

CERUMENEX

Product Number

2

Dosage Form

-

Strength

10%

Approval Date

1982-01-01

11340 / 2

Active Ingredient

TROLAMINE POLYPEPTIDE OLEATE CONDENSATE

Application Number

11340

Product Number

2

Dosage Form

-

Strength

10%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1986
04 Mar
Discontinued Application: 88584

Drug Name

DHC PLUS

Product Number

1

Dosage Form

-

Strength

356.4MG;30MG;16MG

Approval Date

1986-03-04

88584 / 1

Active Ingredient

ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE

Application Number

88584

Product Number

1

Dosage Form

-

Strength

356.4MG;30MG;16MG

Approval Date

1986-03-04

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 11695

Drug Name

PHENY-PAS-TEBAMIN

Product Number

2

Dosage Form

-

Strength

50%

Approval Date

1982-01-01

11695 / 2

Active Ingredient

PHENYL AMINOSALICYLATE

Application Number

11695

Product Number

2

Dosage Form

-

Strength

50%

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 11695

Drug Name

PHENY-PAS-TEBAMIN

Product Number

3

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

11695 / 3

Active Ingredient

PHENYL AMINOSALICYLATE

Application Number

11695

Product Number

3

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 86760

Drug Name

PHYLLOCONTIN

Product Number

1

Dosage Form

-

Strength

225MG

Approval Date

1982-01-01

86760 / 1

Active Ingredient

AMINOPHYLLINE

Application Number

86760

Product Number

1

Dosage Form

-

Strength

225MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 13093

Drug Name

SULFABID

Product Number

1

Dosage Form

-

Strength

500MG/5ML

Approval Date

1982-01-01

13093 / 1

Active Ingredient

SULFAPHENAZOLE

Application Number

13093

Product Number

1

Dosage Form

-

Strength

500MG/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1983
17 Aug
Discontinued Application: 88253

Drug Name

T-PHYL

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1983-08-17

88253 / 1

Active Ingredient

THEOPHYLLINE

Application Number

88253

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1983-08-17

Regulatory Status

Discontinued

Related Databases
  • FDA Inspections
    19 View
  • EDQM CEP
    0 View
  • KDMF
    0 View
  • Japan DMF
    0 View
  • Eudra GMP
    0 View
  • NDC Database
    0 View
  • FDA Approved Drugs Database
    15 View
  • Drug Prices in Switzerland
    0 View
Drug Status Breakdown
15 total
  • Discontinued
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

ATHROMBIN

Application Number

11771

Product Number

1

Active Ingredient

WARFARIN SODIUM

Dosage Form

-

Strength

25MG

FDA Approved Drug Data

Approved drug product information

Regular Updates

Data maintained from official sources

Structured Database

Searchable pharmaceutical data

Reliable Data

Organized FDA drug records

Create a New Buying Request

Fields marked with * are mandatory.

Please enter quantity.
Please select a unit.
Please select quality standard.
Please select request type.
Please provide product specifications.
Please enter additional details.
Please select shipping preference.
Notice: By submitting this buying request, the provided product details and requirements may be published publicly on our marketplace.
Login to Submit