Pharmaco Discontinued
FDA Approved Drugs

Pharmaco 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 Aug 03, 2012
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
15
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Discontinued
6
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RX
9
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Company Overview

Company

Pharmaco Discontinued

Country

Australia

Website

Visit Website

Email

enquiries@pharmaco.com.au

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Company Snapshot

Pharmaco Discontinued

Locked Bag 1009 Gordon NSW 2072

Australia

pharmaco.com.au/ enquiries@pharmaco.com.au View on Map
FDA Approved Drug Records ( 6 records )
1988
17 Aug
Discontinued Application: 72267

Drug Name

FENOPROFEN CALCIUM

Product Number

1

Dosage Form

-

Strength

EQ 600MG BASE

Approval Date

1988-08-17

72267 / 1

Active Ingredient

FENOPROFEN CALCIUM

Application Number

72267

Product Number

1

Dosage Form

-

Strength

EQ 600MG BASE

Approval Date

1988-08-17

Regulatory Status

Discontinued

2012
03 Aug
Discontinued Application: 91588

Drug Name

MONTELUKAST SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 4MG BASE

Approval Date

2012-08-03

91588 / 1

Active Ingredient

MONTELUKAST SODIUM

Application Number

91588

Product Number

1

Dosage Form

-

Strength

EQ 4MG BASE

Approval Date

2012-08-03

Regulatory Status

Discontinued

2012
03 Aug
Discontinued Application: 91588

Drug Name

MONTELUKAST SODIUM

Product Number

2

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2012-08-03

91588 / 2

Active Ingredient

MONTELUKAST SODIUM

Application Number

91588

Product Number

2

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2012-08-03

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17604

Drug Name

NALFON

Product Number

2

Dosage Form

-

Strength

EQ 300MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

17604 / 2

Active Ingredient

FENOPROFEN CALCIUM

Application Number

17604

Product Number

2

Dosage Form

-

Strength

EQ 300MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17604

Drug Name

NALFON

Product Number

3

Dosage Form

-

Strength

EQ 200MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

17604 / 3

Active Ingredient

FENOPROFEN CALCIUM

Application Number

17604

Product Number

3

Dosage Form

-

Strength

EQ 200MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

Regulatory Status

Discontinued

2009
21 Jul
Discontinued Application: 17604

Drug Name

NALFON

Product Number

4

Dosage Form

-

Strength

EQ 400MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2009-07-21

17604 / 4

Active Ingredient

FENOPROFEN CALCIUM

Application Number

17604

Product Number

4

Dosage Form

-

Strength

EQ 400MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2009-07-21

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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FDA Approved Drug Record Details Preview

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

Drug Name

FENOPROFEN CALCIUM

Application Number

72267

Product Number

1

Active Ingredient

FENOPROFEN CALCIUM

Dosage Form

-

Strength

EQ 600MG BASE

FDA Approved Drug Data

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