Kenton Discontinued
FDA Approved Drugs

Kenton 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 4
  • Latest Approval Date Apr 24, 2015
  • Data Source FDA
  • First Approval Date Apr 30, 1998
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Discontinued
4
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RX
3
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Company Overview

Company

Kenton Discontinued

Country

South Africa

Social Profiles

Company Snapshot

Kenton Discontinued

40 Kenton Rd, Kenton-on-Sea, 6191

South Africa

kenton.co.za/ tourism@kenton.co.za View on Map
FDA Approved Drug Records ( 4 records )
2015
24 Apr
Discontinued Application: 91517

Drug Name

REPAGLINIDE

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

2015-04-24

91517 / 1

Active Ingredient

REPAGLINIDE

Application Number

91517

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

2015-04-24

Regulatory Status

Discontinued

2015
24 Apr
Discontinued Application: 91517

Drug Name

REPAGLINIDE

Product Number

2

Dosage Form

-

Strength

1MG

Approval Date

2015-04-24

91517 / 2

Active Ingredient

REPAGLINIDE

Application Number

91517

Product Number

2

Dosage Form

-

Strength

1MG

Approval Date

2015-04-24

Regulatory Status

Discontinued

2015
24 Apr
Discontinued Application: 91517

Drug Name

REPAGLINIDE

Product Number

3

Dosage Form

-

Strength

2MG

Approval Date

2015-04-24

91517 / 3

Active Ingredient

REPAGLINIDE

Application Number

91517

Product Number

3

Dosage Form

-

Strength

2MG

Approval Date

2015-04-24

Regulatory Status

Discontinued

1998
30 Apr
Discontinued Application: 74912

Drug Name

SELEGILINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1998-04-30

74912 / 1

Active Ingredient

SELEGILINE HYDROCHLORIDE

Application Number

74912

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1998-04-30

Regulatory Status

Discontinued

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Drug Status Breakdown
4 total
  • Discontinued
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

REPAGLINIDE

Application Number

91517

Product Number

1

Active Ingredient

REPAGLINIDE

Dosage Form

-

Strength

0.5MG

FDA Approved Drug Data

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