WILSHIRE PHARMS INC Discontinued
FDA Approved Drugs

WILSHIRE PHARMS INC 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 5
  • Latest Approval Date May 08, 2020
  • Data Source FDA
  • First Approval Date Oct 13, 2017
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Discontinued
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RX
15
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Company Overview

Company

WILSHIRE PHARMS INC Discontinued

Country

U.S.A

Website

Visit Website

Email

swhite@wilshirerx.com

Social Profiles

Company Snapshot

WILSHIRE PHARMS INC Discontinued

Six Concourse Parkway, Suite 1800 Atlanta, GA 30328

U.S.A

wilshirerx.com/ swhite@wilshirerx.com View on Map
FDA Approved Drug Records ( 5 records )
2020
08 May
Discontinued Application: 212791

Drug Name

DEXMEDETOMIDINE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

EQ 80MCG BASE/20ML (EQ 4MCG BASE/ML)

Approval Date

2020-05-08

212791 / 3

Active Ingredient

DEXMEDETOMIDINE HYDROCHLORIDE

Application Number

212791

Product Number

3

Dosage Form

-

Strength

EQ 80MCG BASE/20ML (EQ 4MCG BASE/ML)

Approval Date

2020-05-08

Regulatory Status

Discontinued

2017
13 Oct
Discontinued Application: 206857

Drug Name

TIAGABINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

2017-10-13

206857 / 1

Active Ingredient

TIAGABINE HYDROCHLORIDE

Application Number

206857

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

2017-10-13

Regulatory Status

Discontinued

2017
13 Oct
Discontinued Application: 206857

Drug Name

TIAGABINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

4MG

Approval Date

2017-10-13

206857 / 2

Active Ingredient

TIAGABINE HYDROCHLORIDE

Application Number

206857

Product Number

2

Dosage Form

-

Strength

4MG

Approval Date

2017-10-13

Regulatory Status

Discontinued

2017
13 Oct
Discontinued Application: 206857

Drug Name

TIAGABINE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

12MG

Approval Date

2017-10-13

206857 / 3

Active Ingredient

TIAGABINE HYDROCHLORIDE

Application Number

206857

Product Number

3

Dosage Form

-

Strength

12MG

Approval Date

2017-10-13

Regulatory Status

Discontinued

2017
13 Oct
Discontinued Application: 206857

Drug Name

TIAGABINE HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

16MG

Approval Date

2017-10-13

206857 / 4

Active Ingredient

TIAGABINE HYDROCHLORIDE

Application Number

206857

Product Number

4

Dosage Form

-

Strength

16MG

Approval Date

2017-10-13

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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FDA Approved Drug Record Details Preview

Explore important FDA approved drug information available in the records above.

Drug Name

DEXMEDETOMIDINE HYDROCHLORIDE

Application Number

212791

Product Number

3

Active Ingredient

DEXMEDETOMIDINE HYDROCHLORIDE

Dosage Form

-

Strength

EQ 80MCG BASE/20ML (EQ 4MCG BASE/ML)

FDA Approved Drug Data

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