GUERBET Discontinued
FDA Approved Drugs

GUERBET Discontinued

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 3
  • Latest Approval Date Dec 21, 1995
  • Data Source FDA
  • First Approval Date Jul 26, 1985
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Discontinued
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RX
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Company Overview

Company

GUERBET Discontinued

Country

France

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Email

customer.service-us(at)guerbet-group.com

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Company Snapshot

GUERBET Discontinued

15 rue des Vanesses Zone Paris Nord II 93420 Villepinte

France

www.guerbet.com/ customer.service-us(at)guerbet-group.com View on Map
FDA Approved Drug Records ( 3 records )
1985
26 Jul
Discontinued Application: 18905

Drug Name

HEXABRIX

Product Number

2

Dosage Form

-

Strength

39.3%;19.6%

Approval Date

1985-07-26

18905 / 2

Active Ingredient

IOXAGLATE MEGLUMINE; IOXAGLATE SODIUM

Application Number

18905

Product Number

2

Dosage Form

-

Strength

39.3%;19.6%

Approval Date

1985-07-26

Regulatory Status

Discontinued

1995
21 Dec
Discontinued Application: 20316

Drug Name

OXILAN-300

Product Number

1

Dosage Form

-

Strength

62%

Approval Date

1995-12-21

20316 / 1

Active Ingredient

IOXILAN

Application Number

20316

Product Number

1

Dosage Form

-

Strength

62%

Approval Date

1995-12-21

Regulatory Status

Discontinued

1995
21 Dec
Discontinued Application: 20316

Drug Name

OXILAN-350

Product Number

2

Dosage Form

-

Strength

73%

Approval Date

1995-12-21

20316 / 2

Active Ingredient

IOXILAN

Application Number

20316

Product Number

2

Dosage Form

-

Strength

73%

Approval Date

1995-12-21

Regulatory Status

Discontinued

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Drug Status Breakdown
3 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

HEXABRIX

Application Number

18905

Product Number

2

Active Ingredient

IOXAGLATE MEGLUMINE; IOXAGLATE SODIUM

Dosage Form

-

Strength

39.3%;19.6%

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

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