Advanz Pharma
FDA Approved Drugs

Advanz Pharma

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 23
  • Latest Approval Date Jun 01, 2006
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
23
View
Discontinued
7
View
RX
16
View
Company Overview

Company

Advanz Pharma

Country

United Kingdom

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Company Snapshot

Advanz Pharma

11-15 Seaton Place St Helier Jersey JE4 0QH

United Kingdom

www.advanzpharma.com/ View on Map
FDA Approved Drug Records ( 23 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

1982
01 Jan
RX Application: 13174

Drug Name

DYRENIUM

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

13174 / 1

Active Ingredient

TRIAMTERENE

Application Number

13174

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

RX

1982
01 Jan
RX Application: 13174

Drug Name

DYRENIUM

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

13174 / 2

Active Ingredient

TRIAMTERENE

Application Number

13174

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

RX

1997
30 Sep
RX Application: 20405

Drug Name

LANOXIN

Product Number

1

Dosage Form

-

Strength

0.0625MG

Approval Date

1997-09-30

20405 / 1

Active Ingredient

DIGOXIN

Application Number

20405

Product Number

1

Dosage Form

-

Strength

0.0625MG

Approval Date

1997-09-30

Regulatory Status

RX

1997
30 Sep
RX Application: 20405

Drug Name

LANOXIN

Product Number

2

Dosage Form

-

Strength

0.125MG

Approval Date

1997-09-30

20405 / 2

Active Ingredient

DIGOXIN

Application Number

20405

Product Number

2

Dosage Form

-

Strength

0.125MG

Approval Date

1997-09-30

Regulatory Status

RX

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
RX Application: 20405

Drug Name

LANOXIN

Product Number

4

Dosage Form

-

Strength

0.25MG

Approval Date

1997-09-30

20405 / 4

Active Ingredient

DIGOXIN

Application Number

20405

Product Number

4

Dosage Form

-

Strength

0.25MG

Approval Date

1997-09-30

Regulatory Status

RX

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

2006
01 Jun
RX Application: 21959

Drug Name

ORAPRED ODT

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2006-06-01

21959 / 1

Active Ingredient

PREDNISOLONE SODIUM PHOSPHATE

Application Number

21959

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2006-06-01

Regulatory Status

RX

2006
01 Jun
RX Application: 21959

Drug Name

ORAPRED ODT

Product Number

2

Dosage Form

-

Strength

EQ 15MG BASE

Approval Date

2006-06-01

21959 / 2

Active Ingredient

PREDNISOLONE SODIUM PHOSPHATE

Application Number

21959

Product Number

2

Dosage Form

-

Strength

EQ 15MG BASE

Approval Date

2006-06-01

Regulatory Status

RX

2006
01 Jun
RX Application: 21959

Drug Name

ORAPRED ODT

Product Number

3

Dosage Form

-

Strength

EQ 30MG BASE

Approval Date

2006-06-01

21959 / 3

Active Ingredient

PREDNISOLONE SODIUM PHOSPHATE

Application Number

21959

Product Number

3

Dosage Form

-

Strength

EQ 30MG BASE

Approval Date

2006-06-01

Regulatory Status

RX

1999
02 Feb
RX Application: 20886

Drug Name

PANRETIN

Product Number

1

Dosage Form

-

Strength

EQ 0.1% BASE

Approval Date

1999-02-02

20886 / 1

Active Ingredient

ALITRETINOIN

Application Number

20886

Product Number

1

Dosage Form

-

Strength

EQ 0.1% BASE

Approval Date

1999-02-02

Regulatory Status

RX

1985
16 Aug
RX Application: 12342

Drug Name

PARNATE

Product Number

3

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

1985-08-16

12342 / 3

Active Ingredient

TRANYLCYPROMINE SULFATE

Application Number

12342

Product Number

3

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

1985-08-16

Regulatory Status

RX

1982
01 Jan
RX Application: 9768

Drug Name

PLAQUENIL

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

9768 / 1

Active Ingredient

HYDROXYCHLOROQUINE SULFATE

Application Number

9768

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

Regulatory Status

RX

1994
22 Mar
RX Application: 20237

Drug Name

SALAGEN

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1994-03-22

20237 / 1

Active Ingredient

PILOCARPINE HYDROCHLORIDE

Application Number

20237

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1994-03-22

Regulatory Status

RX

2003
18 Apr
RX Application: 20237

Drug Name

SALAGEN

Product Number

2

Dosage Form

-

Strength

7.5MG

Approval Date

2003-04-18

20237 / 2

Active Ingredient

PILOCARPINE HYDROCHLORIDE

Application Number

20237

Product Number

2

Dosage Form

-

Strength

7.5MG

Approval Date

2003-04-18

Regulatory Status

RX

2003
12 Jun
RX Application: 21287

Drug Name

UROXATRAL

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2003-06-12

21287 / 1

Active Ingredient

ALFUZOSIN HYDROCHLORIDE

Application Number

21287

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2003-06-12

Regulatory Status

RX

2000
27 Mar
RX Application: 20789

Drug Name

ZONEGRAN

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2000-03-27

20789 / 1

Active Ingredient

ZONISAMIDE

Application Number

20789

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2000-03-27

Regulatory Status

RX

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

2003
22 Aug
RX Application: 20789

Drug Name

ZONEGRAN

Product Number

3

Dosage Form

-

Strength

25MG

Approval Date

2003-08-22

20789 / 3

Active Ingredient

ZONISAMIDE

Application Number

20789

Product Number

3

Dosage Form

-

Strength

25MG

Approval Date

2003-08-22

Regulatory Status

RX

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Drug Status Breakdown
23 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

DIBENZYLINE

Application Number

8708

Product Number

1

Active Ingredient

PHENOXYBENZAMINE HYDROCHLORIDE

Dosage Form

-

Strength

10MG

FDA Approved Drug Data

Approved drug product information

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