Eurofarma Discontinued
FDA Approved Drugs

Eurofarma 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 Jun 29, 2007
  • Data Source FDA
  • First Approval Date Jan 01, 1982
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14
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Discontinued
3
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RX
11
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Company Overview

Company

Eurofarma Discontinued

Country

Brazil

Social Profiles

Company Snapshot

Eurofarma Discontinued

Rodovia Castelo Branco, 3.565 - Bairro do Itaqui - Itapevi - SP - CEP: 06696-000

Brazil

www.eurofarma.com.br/es/quien-somos/ euroatende@eurofarma.com.br View on Map
FDA Approved Drug Records ( 3 records )
2007
29 Jun
Discontinued Application: 65316

Drug Name

AMPICILLIN AND SULBACTAM

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL;EQ 500MG BASE/VIAL

Approval Date

2007-06-29

65316 / 1

Active Ingredient

AMPICILLIN SODIUM; SULBACTAM SODIUM

Application Number

65316

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL;EQ 500MG BASE/VIAL

Approval Date

2007-06-29

Regulatory Status

Discontinued

2007
29 Jun
Discontinued Application: 65316

Drug Name

AMPICILLIN AND SULBACTAM

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL;EQ 1GM BASE/VIAL

Approval Date

2007-06-29

65316 / 2

Active Ingredient

AMPICILLIN SODIUM; SULBACTAM SODIUM

Application Number

65316

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL;EQ 1GM BASE/VIAL

Approval Date

2007-06-29

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 16161

Drug Name

SYNALAR-HP

Product Number

2

Dosage Form

-

Strength

0.2%

Approval Date

1982-01-01

16161 / 2

Active Ingredient

FLUOCINOLONE ACETONIDE

Application Number

16161

Product Number

2

Dosage Form

-

Strength

0.2%

Approval Date

1982-01-01

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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Explore important FDA approved drug information available in the records above.

Drug Name

AMPICILLIN AND SULBACTAM

Application Number

65316

Product Number

1

Active Ingredient

AMPICILLIN SODIUM; SULBACTAM SODIUM

Dosage Form

-

Strength

EQ 1GM BASE/VIAL;EQ 500MG BASE/VIAL

FDA Approved Drug Data

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