Recordati Discontinued
FDA Approved Drugs

Recordati 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 6
  • Latest Approval Date Mar 06, 2020
  • Data Source FDA
  • First Approval Date Jan 01, 1982
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Discontinued
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Company Overview

Company

Recordati Discontinued

Country

Italy

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Company Snapshot

Recordati Discontinued

Via Matteo Civitali, 1 20148 Milan

Italy

www.recordati.com/en/ svil@recordati.it View on Map
FDA Approved Drug Records ( 6 records )
1982
01 Jan
Discontinued Application: 50682

Drug Name

COSMEGEN

Product Number

1

Dosage Form

-

Strength

0.5MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

50682 / 1

Active Ingredient

DACTINOMYCIN

Application Number

50682

Product Number

1

Dosage Form

-

Strength

0.5MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

Regulatory Status

Discontinued

1985
30 Jan
Discontinued Application: 18878

Drug Name

INDOCIN

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1985-01-30

18878 / 1

Active Ingredient

INDOMETHACIN SODIUM

Application Number

18878

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1985-01-30

Regulatory Status

Discontinued

2020
06 Mar
Discontinued Application: 212801

Drug Name

ISTURISA

Product Number

3

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2020-03-06

212801 / 3

Active Ingredient

OSILODROSTAT PHOSPHATE

Application Number

212801

Product Number

3

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2020-03-06

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 6695

Drug Name

MUSTARGEN

Product Number

1

Dosage Form

-

Strength

10MG/VIAL

Approval Date

1982-01-01

Active Ingredient

MECHLORETHAMINE HYDROCHLORIDE

Application Number

6695

Product Number

1

Dosage Form

-

Strength

10MG/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 10841

Drug Name

PEGANONE

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

10841 / 1

Active Ingredient

ETHOTOIN

Application Number

10841

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 10841

Drug Name

PEGANONE

Product Number

3

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

10841 / 3

Active Ingredient

ETHOTOIN

Application Number

10841

Product Number

3

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

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Drug Status Breakdown
6 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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Explore important FDA approved drug information available in the records above.

Drug Name

COSMEGEN

Application Number

50682

Product Number

1

Active Ingredient

DACTINOMYCIN

Dosage Form

-

Strength

0.5MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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