Noven Pharmaceuticals Discontinued
FDA Approved Drugs

Noven Pharmaceuticals 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 8
  • Latest Approval Date Dec 01, 2020
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
26
View
Unclassified
3
View
Discontinued
8
View
RX
15
View
Company Overview

Company

Noven Pharmaceuticals Discontinued

Country

U.S.A

Website

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Company Snapshot

Noven Pharmaceuticals Discontinued

Noven11960 SW 144th StreetMiami, FL 33186

U.S.A

www.noven.com/ View on Map
FDA Approved Drug Records ( 8 records )
1996
21 May
Discontinued Application: 20575

Drug Name

DENTIPATCH

Product Number

1

Dosage Form

-

Strength

23MG/PATCH

Approval Date

1996-05-21

20575 / 1

Active Ingredient

LIDOCAINE

Application Number

20575

Product Number

1

Dosage Form

-

Strength

23MG/PATCH

Approval Date

1996-05-21

Regulatory Status

Discontinued

1996
21 May
Discontinued Application: 20575

Drug Name

DENTIPATCH

Product Number

2

Dosage Form

-

Strength

46.1MG/PATCH

Approval Date

1996-05-21

20575 / 2

Active Ingredient

LIDOCAINE

Application Number

20575

Product Number

2

Dosage Form

-

Strength

46.1MG/PATCH

Approval Date

1996-05-21

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 16860

Drug Name

ESKALITH

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

1982-01-01

16860 / 1

Active Ingredient

LITHIUM CARBONATE

Application Number

16860

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

2009
16 Oct
Discontinued Application: 77775

Drug Name

FENTANYL-100

Product Number

4

Dosage Form

-

Strength

100MCG/HR

Approval Date

2009-10-16

77775 / 4

Active Ingredient

FENTANYL

Application Number

77775

Product Number

4

Dosage Form

-

Strength

100MCG/HR

Approval Date

2009-10-16

Regulatory Status

Discontinued

2009
16 Oct
Discontinued Application: 77775

Drug Name

FENTANYL-25

Product Number

1

Dosage Form

-

Strength

25MCG/HR

Approval Date

2009-10-16

77775 / 1

Active Ingredient

FENTANYL

Application Number

77775

Product Number

1

Dosage Form

-

Strength

25MCG/HR

Approval Date

2009-10-16

Regulatory Status

Discontinued

2009
16 Oct
Discontinued Application: 77775

Drug Name

FENTANYL-50

Product Number

2

Dosage Form

-

Strength

50MCG/HR

Approval Date

2009-10-16

77775 / 2

Active Ingredient

FENTANYL

Application Number

77775

Product Number

2

Dosage Form

-

Strength

50MCG/HR

Approval Date

2009-10-16

Regulatory Status

Discontinued

2009
16 Oct
Discontinued Application: 77775

Drug Name

FENTANYL-75

Product Number

3

Dosage Form

-

Strength

75MCG/HR

Approval Date

2009-10-16

77775 / 3

Active Ingredient

FENTANYL

Application Number

77775

Product Number

3

Dosage Form

-

Strength

75MCG/HR

Approval Date

2009-10-16

Regulatory Status

Discontinued

2020
01 Dec
Discontinued Application: 203265

Drug Name

LIDOCAINE

Product Number

1

Dosage Form

-

Strength

5%

Approval Date

2020-12-01

203265 / 1

Active Ingredient

LIDOCAINE

Application Number

203265

Product Number

1

Dosage Form

-

Strength

5%

Approval Date

2020-12-01

Regulatory Status

Discontinued

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Drug Status Breakdown
8 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

DENTIPATCH

Application Number

20575

Product Number

1

Active Ingredient

LIDOCAINE

Dosage Form

-

Strength

23MG/PATCH

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