Angelini Pharma
FDA Approved Drugs

Angelini Pharma

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 2
  • Latest Approval Date Feb 02, 2010
  • Data Source FDA
  • First Approval Date Feb 02, 2010
Company Overview

Company

Angelini Pharma

Country

Italy

Social Profiles

LinkedIn
Company Snapshot

Angelini Pharma

Via Guardapasso, 1 - 04011 Aprilia (LT) Italy

Italy

www.angelinifinechemicals.com/ finechemicals@angeliniphama.com View on Map
FDA Approved Drug Records ( 2 records )
2010
02 Feb
Discontinued Application: 22411

Drug Name

OLEPTRO

Product Number

1

Dosage Form

-

Strength

150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2010-02-02

22411 / 1

Active Ingredient

TRAZODONE HYDROCHLORIDE

Application Number

22411

Product Number

1

Dosage Form

-

Strength

150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2010-02-02

Regulatory Status

Discontinued

2010
02 Feb
Discontinued Application: 22411

Drug Name

OLEPTRO

Product Number

2

Dosage Form

-

Strength

300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2010-02-02

22411 / 2

Active Ingredient

TRAZODONE HYDROCHLORIDE

Application Number

22411

Product Number

2

Dosage Form

-

Strength

300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2010-02-02

Regulatory Status

Discontinued

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Drug Status Breakdown
2 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

OLEPTRO

Application Number

22411

Product Number

1

Active Ingredient

TRAZODONE HYDROCHLORIDE

Dosage Form

-

Strength

150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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