Gedeon Richter
FDA Approved Drugs

Gedeon Richter

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 9
  • Latest Approval Date Jul 17, 2007
  • Data Source FDA
  • First Approval Date Jul 29, 2004
Company Overview

Company

Gedeon Richter

Country

Hungary

Website

Visit Website

Email

posta@richter.hu

Social Profiles

Company Snapshot

Gedeon Richter

1103, Gyömrői road 19-21,Budapest

Hungary

www.richter.hu/hu-HU/Pages/default.aspx posta@richter.hu View on Map
FDA Approved Drug Records ( 9 records )
2007
17 Jul
Discontinued Application: 77333

Drug Name

AMLODIPINE BESYLATE

Product Number

1

Dosage Form

-

Strength

EQ 2.5MG BASE

Approval Date

2007-07-17

77333 / 1

Active Ingredient

AMLODIPINE BESYLATE

Application Number

77333

Product Number

1

Dosage Form

-

Strength

EQ 2.5MG BASE

Approval Date

2007-07-17

Regulatory Status

Discontinued

2007
17 Jul
Discontinued Application: 77333

Drug Name

AMLODIPINE BESYLATE

Product Number

2

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2007-07-17

77333 / 2

Active Ingredient

AMLODIPINE BESYLATE

Application Number

77333

Product Number

2

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2007-07-17

Regulatory Status

Discontinued

2007
17 Jul
Discontinued Application: 77333

Drug Name

AMLODIPINE BESYLATE

Product Number

3

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2007-07-17

77333 / 3

Active Ingredient

AMLODIPINE BESYLATE

Application Number

77333

Product Number

3

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2007-07-17

Regulatory Status

Discontinued

2006
22 Dec
Discontinued Application: 77251

Drug Name

FINASTERIDE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2006-12-22

77251 / 1

Active Ingredient

FINASTERIDE

Application Number

77251

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2006-12-22

Regulatory Status

Discontinued

2004
29 Jul
Discontinued Application: 76432

Drug Name

FLUCONAZOLE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

2004-07-29

76432 / 1

Active Ingredient

FLUCONAZOLE

Application Number

76432

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

2004-07-29

Regulatory Status

Discontinued

2004
29 Jul
Discontinued Application: 76432

Drug Name

FLUCONAZOLE

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

2004-07-29

76432 / 2

Active Ingredient

FLUCONAZOLE

Application Number

76432

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

2004-07-29

Regulatory Status

Discontinued

2004
29 Jul
Discontinued Application: 76432

Drug Name

FLUCONAZOLE

Product Number

3

Dosage Form

-

Strength

150MG

Approval Date

2004-07-29

76432 / 3

Active Ingredient

FLUCONAZOLE

Application Number

76432

Product Number

3

Dosage Form

-

Strength

150MG

Approval Date

2004-07-29

Regulatory Status

Discontinued

2004
29 Jul
Discontinued Application: 76432

Drug Name

FLUCONAZOLE

Product Number

4

Dosage Form

-

Strength

200MG

Approval Date

2004-07-29

76432 / 4

Active Ingredient

FLUCONAZOLE

Application Number

76432

Product Number

4

Dosage Form

-

Strength

200MG

Approval Date

2004-07-29

Regulatory Status

Discontinued

2007
02 Jul
Discontinued Application: 77065

Drug Name

TERBINAFINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

2007-07-02

77065 / 1

Active Ingredient

TERBINAFINE HYDROCHLORIDE

Application Number

77065

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

2007-07-02

Regulatory Status

Discontinued

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Drug Status Breakdown
9 total
  • Discontinued
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

AMLODIPINE BESYLATE

Application Number

77333

Product Number

1

Active Ingredient

AMLODIPINE BESYLATE

Dosage Form

-

Strength

EQ 2.5MG BASE

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

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