Advanz Pharma Discontinued
FDA Approved Drugs

Advanz Pharma 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 7
  • Latest Approval Date Aug 22, 2003
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
23
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Discontinued
7
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RX
16
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Company Overview

Company

Advanz Pharma Discontinued

Country

United Kingdom

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Company Snapshot

Advanz Pharma Discontinued

11-15 Seaton Place St Helier Jersey JE4 0QH

United Kingdom

www.advanzpharma.com/ View on Map
FDA Approved Drug Records ( 7 records )
1982
01 Jan
Discontinued Application: 8708

Drug Name

DIBENZYLINE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

8708 / 1

Active Ingredient

PHENOXYBENZAMINE HYDROCHLORIDE

Application Number

8708

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1997
30 Sep
Discontinued Application: 20405

Drug Name

LANOXIN

Product Number

3

Dosage Form

-

Strength

0.1875MG

Approval Date

1997-09-30

20405 / 3

Active Ingredient

DIGOXIN

Application Number

20405

Product Number

3

Dosage Form

-

Strength

0.1875MG

Approval Date

1997-09-30

Regulatory Status

Discontinued

1997
30 Sep
Discontinued Application: 20405

Drug Name

LANOXIN

Product Number

5

Dosage Form

-

Strength

0.375MG

Approval Date

1997-09-30

20405 / 5

Active Ingredient

DIGOXIN

Application Number

20405

Product Number

5

Dosage Form

-

Strength

0.375MG

Approval Date

1997-09-30

Regulatory Status

Discontinued

1997
30 Sep
Discontinued Application: 20405

Drug Name

LANOXIN

Product Number

6

Dosage Form

-

Strength

0.5MG

Approval Date

1997-09-30

20405 / 6

Active Ingredient

DIGOXIN

Application Number

20405

Product Number

6

Dosage Form

-

Strength

0.5MG

Approval Date

1997-09-30

Regulatory Status

Discontinued

1996
19 Sep
Discontinued Application: 20169

Drug Name

NILANDRON

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1996-09-19

20169 / 1

Active Ingredient

NILUTAMIDE

Application Number

20169

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1996-09-19

Regulatory Status

Discontinued

1999
30 Apr
Discontinued Application: 20169

Drug Name

NILANDRON

Product Number

2

Dosage Form

-

Strength

150MG

Approval Date

1999-04-30

20169 / 2

Active Ingredient

NILUTAMIDE

Application Number

20169

Product Number

2

Dosage Form

-

Strength

150MG

Approval Date

1999-04-30

Regulatory Status

Discontinued

2003
22 Aug
Discontinued Application: 20789

Drug Name

ZONEGRAN

Product Number

2

Dosage Form

-

Strength

50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2003-08-22

20789 / 2

Active Ingredient

ZONISAMIDE

Application Number

20789

Product Number

2

Dosage Form

-

Strength

50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2003-08-22

Regulatory Status

Discontinued

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Drug Status Breakdown
7 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

DIBENZYLINE

Application Number

8708

Product Number

1

Active Ingredient

PHENOXYBENZAMINE HYDROCHLORIDE

Dosage Form

-

Strength

10MG

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