FineTech Pharmaceutical Ltd.
FDA Approved Drugs

FineTech Pharmaceutical Ltd.

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 4
  • Latest Approval Date Apr 04, 2006
  • Data Source FDA
  • First Approval Date Jan 30, 2002
All
4
View
Discontinued
2
View
RX
2
View
Company Overview

Company

FineTech Pharmaceutical Ltd.

Country

Israel

Website

Visit Website

Email

info@finetechlab.com

Social Profiles

Company Snapshot

FineTech Pharmaceutical Ltd.

33, Hanarkissim Street, Nesher 36608

Israel

finetechlab.com/ info@finetechlab.com View on Map
FDA Approved Drug Records ( 4 records )
2006
04 Apr
Discontinued Application: 77569

Drug Name

ALBUTEROL SULFATE

Product Number

1

Dosage Form

-

Strength

EQ 0.083% BASE

Approval Date

2006-04-04

77569 / 1

Active Ingredient

ALBUTEROL SULFATE

Application Number

77569

Product Number

1

Dosage Form

-

Strength

EQ 0.083% BASE

Approval Date

2006-04-04

Regulatory Status

Discontinued

2002
30 Jan
RX Application: 75464

Drug Name

FLUOXETINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2002-01-30

75464 / 1

Active Ingredient

FLUOXETINE HYDROCHLORIDE

Application Number

75464

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2002-01-30

Regulatory Status

RX

2002
30 Jan
RX Application: 75464

Drug Name

FLUOXETINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2002-01-30

75464 / 2

Active Ingredient

FLUOXETINE HYDROCHLORIDE

Application Number

75464

Product Number

2

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2002-01-30

Regulatory Status

RX

2005
19 Jul
Discontinued Application: 77072

Drug Name

IPRATROPIUM BROMIDE

Product Number

1

Dosage Form

-

Strength

0.02%

Approval Date

2005-07-19

77072 / 1

Active Ingredient

IPRATROPIUM BROMIDE

Application Number

77072

Product Number

1

Dosage Form

-

Strength

0.02%

Approval Date

2005-07-19

Regulatory Status

Discontinued

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Drug Status Breakdown
4 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

ALBUTEROL SULFATE

Application Number

77569

Product Number

1

Active Ingredient

ALBUTEROL SULFATE

Dosage Form

-

Strength

EQ 0.083% BASE

FDA Approved Drug Data

Approved drug product information

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