CONCORDIA PHARMS INC
FDA Approved Drugs

CONCORDIA PHARMS INC

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 5
  • Latest Approval Date Sep 28, 2010
  • Data Source FDA
  • First Approval Date Dec 14, 2000
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CONCORDIA PHARMS INC

Country

Canada

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CONCORDIA PHARMS INC

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FDA Approved Drug Records ( 5 records )
2009
30 Sep
Discontinued Application: 22331

Drug Name

JENLOGA

Product Number

1

Dosage Form

-

Strength

0.1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2009-09-30

22331 / 1

Active Ingredient

CLONIDINE HYDROCHLORIDE

Application Number

22331

Product Number

1

Dosage Form

-

Strength

0.1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2009-09-30

Regulatory Status

Discontinued

2010
25 May
Discontinued Application: 22331

Drug Name

JENLOGA

Product Number

2

Dosage Form

-

Strength

0.2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2010-05-25

22331 / 2

Active Ingredient

CLONIDINE HYDROCHLORIDE

Application Number

22331

Product Number

2

Dosage Form

-

Strength

0.2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2010-05-25

Regulatory Status

Discontinued

2010
28 Sep
Discontinued Application: 22331

Drug Name

KAPVAY

Product Number

3

Dosage Form

-

Strength

0.1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2010-09-28

22331 / 3

Active Ingredient

CLONIDINE HYDROCHLORIDE

Application Number

22331

Product Number

3

Dosage Form

-

Strength

0.1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2010-09-28

Regulatory Status

Discontinued

2010
28 Sep
Discontinued Application: 22331

Drug Name

KAPVAY

Product Number

4

Dosage Form

-

Strength

0.2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2010-09-28

22331 / 4

Active Ingredient

CLONIDINE HYDROCHLORIDE

Application Number

22331

Product Number

4

Dosage Form

-

Strength

0.2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2010-09-28

Regulatory Status

Discontinued

2000
14 Dec
Discontinued Application: 75117

Drug Name

ORAPRED

Product Number

1

Dosage Form

-

Strength

EQ 15MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2000-12-14

75117 / 1

Active Ingredient

PREDNISOLONE SODIUM PHOSPHATE

Application Number

75117

Product Number

1

Dosage Form

-

Strength

EQ 15MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2000-12-14

Regulatory Status

Discontinued

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Drug Status Breakdown
5 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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Explore important FDA approved drug information available in the records above.

Drug Name

JENLOGA

Application Number

22331

Product Number

1

Active Ingredient

CLONIDINE HYDROCHLORIDE

Dosage Form

-

Strength

0.1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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