New River Pharmaceuticals Inc.
FDA Approved Drugs

New River Pharmaceuticals 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 12
  • Latest Approval Date Apr 13, 1987
  • Data Source FDA
  • First Approval Date Jan 01, 1982
Company Overview

Company

New River Pharmaceuticals Inc.

Country

U.S.A

Website

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Company Snapshot

New River Pharmaceuticals Inc.

The Governor Tyler 1881 Grove Avenue Radford, VA 24141

U.S.A

www.nrpharma.com/ View on Map
FDA Approved Drug Records ( 12 records )
1982
01 Jan
Discontinued Application: 16987

Drug Name

DOXEPIN HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

1982-01-01

16987 / 1

Active Ingredient

DOXEPIN HYDROCHLORIDE

Application Number

16987

Product Number

1

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 16987

Drug Name

DOXEPIN HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 25MG BASE

Approval Date

1982-01-01

16987 / 2

Active Ingredient

DOXEPIN HYDROCHLORIDE

Application Number

16987

Product Number

2

Dosage Form

-

Strength

EQ 25MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 16987

Drug Name

DOXEPIN HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

1982-01-01

16987 / 3

Active Ingredient

DOXEPIN HYDROCHLORIDE

Application Number

16987

Product Number

3

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 16987

Drug Name

DOXEPIN HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

1982-01-01

16987 / 4

Active Ingredient

DOXEPIN HYDROCHLORIDE

Application Number

16987

Product Number

4

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 16987

Drug Name

DOXEPIN HYDROCHLORIDE

Product Number

6

Dosage Form

-

Strength

EQ 75MG BASE

Approval Date

1982-01-01

16987 / 6

Active Ingredient

DOXEPIN HYDROCHLORIDE

Application Number

16987

Product Number

6

Dosage Form

-

Strength

EQ 75MG BASE

Approval Date

1982-01-01

Regulatory Status

Discontinued

1987
13 Apr
Discontinued Application: 16987

Drug Name

DOXEPIN HYDROCHLORIDE

Product Number

7

Dosage Form

-

Strength

EQ 150MG BASE

Approval Date

1987-04-13

16987 / 7

Active Ingredient

DOXEPIN HYDROCHLORIDE

Application Number

16987

Product Number

7

Dosage Form

-

Strength

EQ 150MG BASE

Approval Date

1987-04-13

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17807

Drug Name

PROFERDEX

Product Number

1

Dosage Form

-

Strength

EQ 50MG IRON/ML

Approval Date

1982-01-01

17807 / 1

Active Ingredient

IRON DEXTRAN

Application Number

17807

Product Number

1

Dosage Form

-

Strength

EQ 50MG IRON/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 14715

Drug Name

TRIAVIL 2-10

Product Number

4

Dosage Form

-

Strength

10MG;2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

14715 / 4

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE

Application Number

14715

Product Number

4

Dosage Form

-

Strength

10MG;2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 14715

Drug Name

TRIAVIL 2-25

Product Number

2

Dosage Form

-

Strength

25MG;2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

14715 / 2

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE

Application Number

14715

Product Number

2

Dosage Form

-

Strength

25MG;2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 14715

Drug Name

TRIAVIL 4-10

Product Number

3

Dosage Form

-

Strength

10MG;4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

14715 / 3

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE

Application Number

14715

Product Number

3

Dosage Form

-

Strength

10MG;4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 14715

Drug Name

TRIAVIL 4-25

Product Number

5

Dosage Form

-

Strength

25MG;4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

14715 / 5

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE

Application Number

14715

Product Number

5

Dosage Form

-

Strength

25MG;4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 14715

Drug Name

TRIAVIL 4-50

Product Number

6

Dosage Form

-

Strength

50MG;4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

14715 / 6

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE

Application Number

14715

Product Number

6

Dosage Form

-

Strength

50MG;4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

Regulatory Status

Discontinued

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Drug Status Breakdown
12 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

DOXEPIN HYDROCHLORIDE

Application Number

16987

Product Number

1

Active Ingredient

DOXEPIN HYDROCHLORIDE

Dosage Form

-

Strength

EQ 10MG BASE

FDA Approved Drug Data

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