Eurofarma
FDA Approved Drugs

Eurofarma

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 RX
  • Total Records 14
  • Latest Approval Date Jun 30, 2008
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
14
View
Discontinued
3
View
RX
11
View
Company Overview

Company

Eurofarma

Country

Brazil

Website

Visit Website

Email

euroatende@eurofarma.com.br

Social Profiles

Company Snapshot

Eurofarma

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 ( 14 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

2001
12 Apr
RX Application: 75630

Drug Name

BETAXOLOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 0.5% BASE

Approval Date

2001-04-12

75630 / 1

Active Ingredient

BETAXOLOL HYDROCHLORIDE

Application Number

75630

Product Number

1

Dosage Form

-

Strength

EQ 0.5% BASE

Approval Date

2001-04-12

Regulatory Status

RX

1982
30 Dec
RX Application: 18748

Drug Name

LOPROX

Product Number

1

Dosage Form

-

Strength

0.77%

Approval Date

1982-12-30

18748 / 1

Active Ingredient

CICLOPIROX

Application Number

18748

Product Number

1

Dosage Form

-

Strength

0.77%

Approval Date

1982-12-30

Regulatory Status

RX

1988
30 Dec
RX Application: 19824

Drug Name

LOPROX

Product Number

1

Dosage Form

-

Strength

0.77%

Approval Date

1988-12-30

19824 / 1

Active Ingredient

CICLOPIROX

Application Number

19824

Product Number

1

Dosage Form

-

Strength

0.77%

Approval Date

1988-12-30

Regulatory Status

RX

1982
01 Jan
RX Application: 60700

Drug Name

NEO-SYNALAR

Product Number

1

Dosage Form

-

Strength

0.025%;EQ 3.5MG BASE/GM

Approval Date

1982-01-01

60700 / 1

Active Ingredient

FLUOCINOLONE ACETONIDE; NEOMYCIN SULFATE

Application Number

60700

Product Number

1

Dosage Form

-

Strength

0.025%;EQ 3.5MG BASE/GM

Approval Date

1982-01-01

Regulatory Status

RX

1982
01 Jan
RX Application: 12787

Drug Name

SYNALAR

Product Number

2

Dosage Form

-

Strength

0.025%

Approval Date

1982-01-01

12787 / 2

Active Ingredient

FLUOCINOLONE ACETONIDE

Application Number

12787

Product Number

2

Dosage Form

-

Strength

0.025%

Approval Date

1982-01-01

Regulatory Status

RX

1982
01 Jan
RX Application: 12787

Drug Name

SYNALAR

Product Number

4

Dosage Form

-

Strength

0.01%

Approval Date

1982-01-01

12787 / 4

Active Ingredient

FLUOCINOLONE ACETONIDE

Application Number

12787

Product Number

4

Dosage Form

-

Strength

0.01%

Approval Date

1982-01-01

Regulatory Status

RX

1982
01 Jan
RX Application: 12787

Drug Name

SYNALAR

Product Number

5

Dosage Form

-

Strength

0.025%

Approval Date

1982-01-01

12787 / 5

Active Ingredient

FLUOCINOLONE ACETONIDE

Application Number

12787

Product Number

5

Dosage Form

-

Strength

0.025%

Approval Date

1982-01-01

Regulatory Status

RX

1982
01 Jan
RX Application: 13960

Drug Name

SYNALAR

Product Number

1

Dosage Form

-

Strength

0.025%

Approval Date

1982-01-01

13960 / 1

Active Ingredient

FLUOCINOLONE ACETONIDE

Application Number

13960

Product Number

1

Dosage Form

-

Strength

0.025%

Approval Date

1982-01-01

Regulatory Status

RX

1982
01 Jan
RX Application: 15296

Drug Name

SYNALAR

Product Number

1

Dosage Form

-

Strength

0.01%

Approval Date

1982-01-01

15296 / 1

Active Ingredient

FLUOCINOLONE ACETONIDE

Application Number

15296

Product Number

1

Dosage Form

-

Strength

0.01%

Approval Date

1982-01-01

Regulatory Status

RX

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

2008
30 Jun
RX Application: 65401

Drug Name

VANCOMYCIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

2008-06-30

65401 / 1

Active Ingredient

VANCOMYCIN HYDROCHLORIDE

Application Number

65401

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

2008-06-30

Regulatory Status

RX

2008
30 Jun
RX Application: 65401

Drug Name

VANCOMYCIN HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2008-06-30

65401 / 2

Active Ingredient

VANCOMYCIN HYDROCHLORIDE

Application Number

65401

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2008-06-30

Regulatory Status

RX

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Drug Status Breakdown
14 total
  • Discontinued
  • RX
Official Source

FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.

Visit FDA Orange Book
FDA Approved Drug Record Details Preview

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

Approved drug product information

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