WILSHIRE PHARMS INC
FDA Approved Drugs

WILSHIRE 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.

RX Discontinued
  • Total Records 20
  • Latest Approval Date Dec 07, 2023
  • Data Source FDA
  • First Approval Date Dec 17, 2015
All
20
View
Discontinued
5
View
RX
15
View
Company Overview

Company

WILSHIRE PHARMS INC

Country

U.S.A

Website

Visit Website

Email

swhite@wilshirerx.com

Social Profiles

Company Snapshot

WILSHIRE PHARMS INC

Six Concourse Parkway, Suite 1800 Atlanta, GA 30328

U.S.A

wilshirerx.com/ swhite@wilshirerx.com View on Map
FDA Approved Drug Records ( 20 records )
2022
25 Nov
RX Application: 216815

Drug Name

ARFORMOTEROL TARTRATE

Product Number

1

Dosage Form

-

Strength

EQ 0.015MG BASE/2ML

Approval Date

2022-11-25

216815 / 1

Active Ingredient

ARFORMOTEROL TARTRATE

Application Number

216815

Product Number

1

Dosage Form

-

Strength

EQ 0.015MG BASE/2ML

Approval Date

2022-11-25

Regulatory Status

RX

2021
02 Apr
RX Application: 212296

Drug Name

DEOXYCHOLIC ACID

Product Number

1

Dosage Form

-

Strength

20MG/2ML (10MG/ML)

Approval Date

2021-04-02

212296 / 1

Active Ingredient

DEOXYCHOLIC ACID

Application Number

212296

Product Number

1

Dosage Form

-

Strength

20MG/2ML (10MG/ML)

Approval Date

2021-04-02

Regulatory Status

RX

2019
04 Dec
RX Application: 212791

Drug Name

DEXMEDETOMIDINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 200MCG BASE/50ML (EQ 4MCG BASE/ML)

Approval Date

2019-12-04

212791 / 1

Active Ingredient

DEXMEDETOMIDINE HYDROCHLORIDE

Application Number

212791

Product Number

1

Dosage Form

-

Strength

EQ 200MCG BASE/50ML (EQ 4MCG BASE/ML)

Approval Date

2019-12-04

Regulatory Status

RX

2019
04 Dec
RX Application: 212791

Drug Name

DEXMEDETOMIDINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 400MCG BASE/100ML (EQ 4MCG BASE/ML)

Approval Date

2019-12-04

212791 / 2

Active Ingredient

DEXMEDETOMIDINE HYDROCHLORIDE

Application Number

212791

Product Number

2

Dosage Form

-

Strength

EQ 400MCG BASE/100ML (EQ 4MCG BASE/ML)

Approval Date

2019-12-04

Regulatory Status

RX

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

2022
13 Dec
RX Application: 215621

Drug Name

FORMOTEROL FUMARATE

Product Number

1

Dosage Form

-

Strength

0.02MG/2ML

Approval Date

2022-12-13

215621 / 1

Active Ingredient

FORMOTEROL FUMARATE

Application Number

215621

Product Number

1

Dosage Form

-

Strength

0.02MG/2ML

Approval Date

2022-12-13

Regulatory Status

RX

2020
01 Sep
RX Application: 211501

Drug Name

ICATIBANT ACETATE

Product Number

1

Dosage Form

-

Strength

EQ 30MG BASE/3ML (EQ 10MG BASE/ML)

Approval Date

2020-09-01

211501 / 1

Active Ingredient

ICATIBANT ACETATE

Application Number

211501

Product Number

1

Dosage Form

-

Strength

EQ 30MG BASE/3ML (EQ 10MG BASE/ML)

Approval Date

2020-09-01

Regulatory Status

RX

2020
18 Dec
RX Application: 212706

Drug Name

MERZEE

Product Number

1

Dosage Form

-

Strength

0.02MG;1MG

Approval Date

2020-12-18

212706 / 1

Active Ingredient

ETHINYL ESTRADIOL; NORETHINDRONE ACETATE

Application Number

212706

Product Number

1

Dosage Form

-

Strength

0.02MG;1MG

Approval Date

2020-12-18

Regulatory Status

RX

2023
03 Jan
RX Application: 214870

Drug Name

METHYLPREDNISOLONE ACETATE

Product Number

1

Dosage Form

-

Strength

80MG/ML

Approval Date

2023-01-03

214870 / 1

Active Ingredient

METHYLPREDNISOLONE ACETATE

Application Number

214870

Product Number

1

Dosage Form

-

Strength

80MG/ML

Approval Date

2023-01-03

Regulatory Status

RX

2023
10 May
RX Application: 214870

Drug Name

METHYLPREDNISOLONE ACETATE

Product Number

2

Dosage Form

-

Strength

40MG/ML

Approval Date

2023-05-10

214870 / 2

Active Ingredient

METHYLPREDNISOLONE ACETATE

Application Number

214870

Product Number

2

Dosage Form

-

Strength

40MG/ML

Approval Date

2023-05-10

Regulatory Status

RX

2023
07 Dec
RX Application: 211345

Drug Name

OMEGA-3-ACID ETHYL ESTERS

Product Number

1

Dosage Form

-

Strength

1GM CONTAINS AT LEAST 900MG OF THE ETHYL ESTERS OF OMEGA-3 FATTY ACIDS

Approval Date

2023-12-07

211345 / 1

Active Ingredient

OMEGA-3-ACID ETHYL ESTERS

Application Number

211345

Product Number

1

Dosage Form

-

Strength

1GM CONTAINS AT LEAST 900MG OF THE ETHYL ESTERS OF OMEGA-3 FATTY ACIDS

Approval Date

2023-12-07

Regulatory Status

RX

2015
17 Dec
RX Application: 205973

Drug Name

PERPHENAZINE

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

2015-12-17

205973 / 1

Active Ingredient

PERPHENAZINE

Application Number

205973

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

2015-12-17

Regulatory Status

RX

2015
17 Dec
RX Application: 205973

Drug Name

PERPHENAZINE

Product Number

2

Dosage Form

-

Strength

4MG

Approval Date

2015-12-17

205973 / 2

Active Ingredient

PERPHENAZINE

Application Number

205973

Product Number

2

Dosage Form

-

Strength

4MG

Approval Date

2015-12-17

Regulatory Status

RX

2015
17 Dec
RX Application: 205973

Drug Name

PERPHENAZINE

Product Number

3

Dosage Form

-

Strength

8MG

Approval Date

2015-12-17

205973 / 3

Active Ingredient

PERPHENAZINE

Application Number

205973

Product Number

3

Dosage Form

-

Strength

8MG

Approval Date

2015-12-17

Regulatory Status

RX

2015
17 Dec
RX Application: 205973

Drug Name

PERPHENAZINE

Product Number

4

Dosage Form

-

Strength

16MG

Approval Date

2015-12-17

205973 / 4

Active Ingredient

PERPHENAZINE

Application Number

205973

Product Number

4

Dosage Form

-

Strength

16MG

Approval Date

2015-12-17

Regulatory Status

RX

2019
24 Apr
RX Application: 206368

Drug Name

TESTOSTERONE CYPIONATE

Product Number

1

Dosage Form

-

Strength

200MG/ML

Approval Date

2019-04-24

206368 / 1

Active Ingredient

TESTOSTERONE CYPIONATE

Application Number

206368

Product Number

1

Dosage Form

-

Strength

200MG/ML

Approval Date

2019-04-24

Regulatory Status

RX

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
20 total
  • RX
  • 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

ARFORMOTEROL TARTRATE

Application Number

216815

Product Number

1

Active Ingredient

ARFORMOTEROL TARTRATE

Dosage Form

-

Strength

EQ 0.015MG BASE/2ML

FDA Approved Drug Data

Approved drug product information

Regular Updates

Data maintained from official sources

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