Mayne Pharma Discontinued
FDA Approved Drugs

Mayne 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 14
  • Latest Approval Date May 24, 2018
  • Data Source FDA
  • First Approval Date Jul 22, 1985
All
27
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Discontinued
14
View
RX
13
View
Company Overview

Company

Mayne Pharma Discontinued

Country

Australia

Website

Visit Website

Email

bd@maynepharma.com

Social Profiles

Company Snapshot

Mayne Pharma Discontinued

1538 Main North Road, Salisbury South, SA 5106

Australia

www.maynepharma.com/ bd@maynepharma.com View on Map
FDA Approved Drug Records ( 14 records )
1985
22 Jul
Discontinued Application: 50582

Drug Name

DORYX

Product Number

1

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

1985-07-22

50582 / 1

Active Ingredient

DOXYCYCLINE HYCLATE

Application Number

50582

Product Number

1

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

1985-07-22

Regulatory Status

Discontinued

2001
13 Aug
Discontinued Application: 50582

Drug Name

DORYX

Product Number

2

Dosage Form

-

Strength

EQ 75MG BASE

Approval Date

2001-08-13

50582 / 2

Active Ingredient

DOXYCYCLINE HYCLATE

Application Number

50582

Product Number

2

Dosage Form

-

Strength

EQ 75MG BASE

Approval Date

2001-08-13

Regulatory Status

Discontinued

2005
06 May
Discontinued Application: 50795

Drug Name

DORYX

Product Number

1

Dosage Form

-

Strength

EQ 75MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2005-05-06

50795 / 1

Active Ingredient

DOXYCYCLINE HYCLATE

Application Number

50795

Product Number

1

Dosage Form

-

Strength

EQ 75MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2005-05-06

Regulatory Status

Discontinued

2005
06 May
Discontinued Application: 50795

Drug Name

DORYX

Product Number

2

Dosage Form

-

Strength

EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2005-05-06

50795 / 2

Active Ingredient

DOXYCYCLINE HYCLATE

Application Number

50795

Product Number

2

Dosage Form

-

Strength

EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2005-05-06

Regulatory Status

Discontinued

2008
20 Jun
Discontinued Application: 50795

Drug Name

DORYX

Product Number

3

Dosage Form

-

Strength

EQ 150MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2008-06-20

50795 / 3

Active Ingredient

DOXYCYCLINE HYCLATE

Application Number

50795

Product Number

3

Dosage Form

-

Strength

EQ 150MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2008-06-20

Regulatory Status

Discontinued

2013
11 Apr
Discontinued Application: 50795

Drug Name

DORYX

Product Number

4

Dosage Form

-

Strength

EQ 80MG BASE

Approval Date

2013-04-11

50795 / 4

Active Ingredient

DOXYCYCLINE HYCLATE

Application Number

50795

Product Number

4

Dosage Form

-

Strength

EQ 80MG BASE

Approval Date

2013-04-11

Regulatory Status

Discontinued

2013
11 Apr
Discontinued Application: 50795

Drug Name

DORYX

Product Number

5

Dosage Form

-

Strength

EQ 200MG BASE

Approval Date

2013-04-11

50795 / 5

Active Ingredient

DOXYCYCLINE HYCLATE

Application Number

50795

Product Number

5

Dosage Form

-

Strength

EQ 200MG BASE

Approval Date

2013-04-11

Regulatory Status

Discontinued

2014
19 Dec
Discontinued Application: 50795

Drug Name

DORYX

Product Number

6

Dosage Form

-

Strength

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

Approval Date

2014-12-19

50795 / 6

Active Ingredient

DOXYCYCLINE HYCLATE

Application Number

50795

Product Number

6

Dosage Form

-

Strength

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

Approval Date

2014-12-19

Regulatory Status

Discontinued

2016
20 May
Discontinued Application: 50795

Drug Name

DORYX MPC

Product Number

8

Dosage Form

-

Strength

EQ 120MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2016-05-20

50795 / 8

Active Ingredient

DOXYCYCLINE HYCLATE

Application Number

50795

Product Number

8

Dosage Form

-

Strength

EQ 120MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2016-05-20

Regulatory Status

Discontinued

2007
20 Aug
Discontinued Application: 77062

Drug Name

FENTANYL-100

Product Number

4

Dosage Form

-

Strength

100MCG/HR

Approval Date

2007-08-20

77062 / 4

Active Ingredient

FENTANYL

Application Number

77062

Product Number

4

Dosage Form

-

Strength

100MCG/HR

Approval Date

2007-08-20

Regulatory Status

Discontinued

2007
20 Aug
Discontinued Application: 77062

Drug Name

FENTANYL-25

Product Number

1

Dosage Form

-

Strength

25MCG/HR

Approval Date

2007-08-20

77062 / 1

Active Ingredient

FENTANYL

Application Number

77062

Product Number

1

Dosage Form

-

Strength

25MCG/HR

Approval Date

2007-08-20

Regulatory Status

Discontinued

2007
20 Aug
Discontinued Application: 77062

Drug Name

FENTANYL-50

Product Number

2

Dosage Form

-

Strength

50MCG/HR

Approval Date

2007-08-20

77062 / 2

Active Ingredient

FENTANYL

Application Number

77062

Product Number

2

Dosage Form

-

Strength

50MCG/HR

Approval Date

2007-08-20

Regulatory Status

Discontinued

2007
20 Aug
Discontinued Application: 77062

Drug Name

FENTANYL-75

Product Number

3

Dosage Form

-

Strength

75MCG/HR

Approval Date

2007-08-20

77062 / 3

Active Ingredient

FENTANYL

Application Number

77062

Product Number

3

Dosage Form

-

Strength

75MCG/HR

Approval Date

2007-08-20

Regulatory Status

Discontinued

2018
24 May
Discontinued Application: 210566

Drug Name

LEXETTE

Product Number

1

Dosage Form

-

Strength

0.05%

Approval Date

2018-05-24

210566 / 1

Active Ingredient

HALOBETASOL PROPIONATE

Application Number

210566

Product Number

1

Dosage Form

-

Strength

0.05%

Approval Date

2018-05-24

Regulatory Status

Discontinued

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Drug Status Breakdown
14 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

DORYX

Application Number

50582

Product Number

1

Active Ingredient

DOXYCYCLINE HYCLATE

Dosage Form

-

Strength

EQ 100MG BASE

FDA Approved Drug Data

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