Prinston Discontinued
FDA Approved Drugs

Prinston 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 22
  • Latest Approval Date Jan 04, 2022
  • Data Source FDA
  • First Approval Date Mar 29, 2002
All
272
View
Unclassified
5
View
Discontinued
22
View
RX
245
View
Company Overview

Company

Prinston Discontinued

Country

U.S.A

Website

Visit Website

Email

contact@prinstonpharm.com

Social Profiles

LinkedIn
Company Snapshot

Prinston Discontinued

700 Atrium Dr. Somerset, New Jersey 08873

U.S.A

www.prinstonpharm.com/ contact@prinstonpharm.com View on Map
FDA Approved Drug Records ( 22 records )
2021
15 Nov
Discontinued Application: 212202

Drug Name

ACYCLOVIR

Product Number

1

Dosage Form

-

Strength

5%

Approval Date

2021-11-15

212202 / 1

Active Ingredient

ACYCLOVIR

Application Number

212202

Product Number

1

Dosage Form

-

Strength

5%

Approval Date

2021-11-15

Regulatory Status

Discontinued

2021
08 Feb
Discontinued Application: 213139

Drug Name

CLOBETASOL PROPIONATE

Product Number

1

Dosage Form

-

Strength

0.05%

Approval Date

2021-02-08

213139 / 1

Active Ingredient

CLOBETASOL PROPIONATE

Application Number

213139

Product Number

1

Dosage Form

-

Strength

0.05%

Approval Date

2021-02-08

Regulatory Status

Discontinued

2019
17 Dec
Discontinued Application: 211223

Drug Name

DOFETILIDE

Product Number

1

Dosage Form

-

Strength

0.125MG

Approval Date

2019-12-17

211223 / 1

Active Ingredient

DOFETILIDE

Application Number

211223

Product Number

1

Dosage Form

-

Strength

0.125MG

Approval Date

2019-12-17

Regulatory Status

Discontinued

2019
17 Dec
Discontinued Application: 211223

Drug Name

DOFETILIDE

Product Number

2

Dosage Form

-

Strength

0.25MG

Approval Date

2019-12-17

211223 / 2

Active Ingredient

DOFETILIDE

Application Number

211223

Product Number

2

Dosage Form

-

Strength

0.25MG

Approval Date

2019-12-17

Regulatory Status

Discontinued

2019
17 Dec
Discontinued Application: 211223

Drug Name

DOFETILIDE

Product Number

3

Dosage Form

-

Strength

0.5MG

Approval Date

2019-12-17

211223 / 3

Active Ingredient

DOFETILIDE

Application Number

211223

Product Number

3

Dosage Form

-

Strength

0.5MG

Approval Date

2019-12-17

Regulatory Status

Discontinued

2017
10 Oct
Discontinued Application: 208782

Drug Name

ENTECAVIR

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

2017-10-10

208782 / 1

Active Ingredient

ENTECAVIR

Application Number

208782

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

2017-10-10

Regulatory Status

Discontinued

2017
10 Oct
Discontinued Application: 208782

Drug Name

ENTECAVIR

Product Number

2

Dosage Form

-

Strength

1MG

Approval Date

2017-10-10

208782 / 2

Active Ingredient

ENTECAVIR

Application Number

208782

Product Number

2

Dosage Form

-

Strength

1MG

Approval Date

2017-10-10

Regulatory Status

Discontinued

2002
29 Mar
Discontinued Application: 40412

Drug Name

HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2002-03-29

40412 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE

Application Number

40412

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

2002-03-29

Regulatory Status

Discontinued

2002
29 Mar
Discontinued Application: 40412

Drug Name

HYDROCHLOROTHIAZIDE

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

2002-03-29

40412 / 2

Active Ingredient

HYDROCHLOROTHIAZIDE

Application Number

40412

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

2002-03-29

Regulatory Status

Discontinued

2021
30 Dec
Discontinued Application: 214928

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

1

Dosage Form

-

Strength

325MG;5MG

Approval Date

2021-12-30

214928 / 1

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

214928

Product Number

1

Dosage Form

-

Strength

325MG;5MG

Approval Date

2021-12-30

Regulatory Status

Discontinued

2021
30 Dec
Discontinued Application: 214928

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

2

Dosage Form

-

Strength

325MG;7.5MG

Approval Date

2021-12-30

214928 / 2

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

214928

Product Number

2

Dosage Form

-

Strength

325MG;7.5MG

Approval Date

2021-12-30

Regulatory Status

Discontinued

2021
30 Dec
Discontinued Application: 214928

Drug Name

HYDROCODONE BITARTRATE AND ACETAMINOPHEN

Product Number

3

Dosage Form

-

Strength

325MG;10MG

Approval Date

2021-12-30

214928 / 3

Active Ingredient

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Application Number

214928

Product Number

3

Dosage Form

-

Strength

325MG;10MG

Approval Date

2021-12-30

Regulatory Status

Discontinued

2012
20 Jul
Discontinued Application: 202533

Drug Name

LEVETIRACETAM

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2012-07-20

202533 / 1

Active Ingredient

LEVETIRACETAM

Application Number

202533

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2012-07-20

Regulatory Status

Discontinued

2012
20 Jul
Discontinued Application: 202533

Drug Name

LEVETIRACETAM

Product Number

2

Dosage Form

-

Strength

750MG

Approval Date

2012-07-20

202533 / 2

Active Ingredient

LEVETIRACETAM

Application Number

202533

Product Number

2

Dosage Form

-

Strength

750MG

Approval Date

2012-07-20

Regulatory Status

Discontinued

2022
04 Jan
Discontinued Application: 210597

Drug Name

METOPROLOL SUCCINATE

Product Number

1

Dosage Form

-

Strength

EQ 100MG TARTRATE

Approval Date

2022-01-04

210597 / 1

Active Ingredient

METOPROLOL SUCCINATE

Application Number

210597

Product Number

1

Dosage Form

-

Strength

EQ 100MG TARTRATE

Approval Date

2022-01-04

Regulatory Status

Discontinued

2022
04 Jan
Discontinued Application: 210597

Drug Name

METOPROLOL SUCCINATE

Product Number

2

Dosage Form

-

Strength

EQ 200MG TARTRATE

Approval Date

2022-01-04

210597 / 2

Active Ingredient

METOPROLOL SUCCINATE

Application Number

210597

Product Number

2

Dosage Form

-

Strength

EQ 200MG TARTRATE

Approval Date

2022-01-04

Regulatory Status

Discontinued

2012
22 May
Discontinued Application: 78644

Drug Name

NEVIRAPINE

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

2012-05-22

78644 / 1

Active Ingredient

NEVIRAPINE

Application Number

78644

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

2012-05-22

Regulatory Status

Discontinued

2010
04 Aug
Discontinued Application: 90027

Drug Name

VENLAFAXINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE

Approval Date

2010-08-04

90027 / 1

Active Ingredient

VENLAFAXINE HYDROCHLORIDE

Application Number

90027

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE

Approval Date

2010-08-04

Regulatory Status

Discontinued

2010
04 Aug
Discontinued Application: 90027

Drug Name

VENLAFAXINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 37.5MG BASE

Approval Date

2010-08-04

90027 / 2

Active Ingredient

VENLAFAXINE HYDROCHLORIDE

Application Number

90027

Product Number

2

Dosage Form

-

Strength

EQ 37.5MG BASE

Approval Date

2010-08-04

Regulatory Status

Discontinued

2010
04 Aug
Discontinued Application: 90027

Drug Name

VENLAFAXINE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

2010-08-04

90027 / 3

Active Ingredient

VENLAFAXINE HYDROCHLORIDE

Application Number

90027

Product Number

3

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

2010-08-04

Regulatory Status

Discontinued

2010
04 Aug
Discontinued Application: 90027

Drug Name

VENLAFAXINE HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

EQ 75MG BASE

Approval Date

2010-08-04

90027 / 4

Active Ingredient

VENLAFAXINE HYDROCHLORIDE

Application Number

90027

Product Number

4

Dosage Form

-

Strength

EQ 75MG BASE

Approval Date

2010-08-04

Regulatory Status

Discontinued

2010
04 Aug
Discontinued Application: 90027

Drug Name

VENLAFAXINE HYDROCHLORIDE

Product Number

5

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

2010-08-04

90027 / 5

Active Ingredient

VENLAFAXINE HYDROCHLORIDE

Application Number

90027

Product Number

5

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

2010-08-04

Regulatory Status

Discontinued

Related Databases
  • FDA Inspections
    0 View
  • EDQM CEP
    0 View
  • KDMF
    0 View
  • Japan DMF
    0 View
  • Eudra GMP
    0 View
  • NDC Database
    0 View
  • FDA Approved Drugs Database
    272 View
  • Drug Prices in Switzerland
    0 View
Drug Status Breakdown
22 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

ACYCLOVIR

Application Number

212202

Product Number

1

Active Ingredient

ACYCLOVIR

Dosage Form

-

Strength

5%

FDA Approved Drug Data

Approved drug product information

Regular Updates

Data maintained from official sources

Structured Database

Searchable pharmaceutical data

Reliable Data

Organized FDA drug records

Create a New Buying Request

Fields marked with * are mandatory.

Please enter quantity.
Please select a unit.
Please select quality standard.
Please select request type.
Please provide product specifications.
Please enter additional details.
Please select shipping preference.
Notice: By submitting this buying request, the provided product details and requirements may be published publicly on our marketplace.
Login to Submit