Promius Pharma
FDA Approved Drugs

Promius Pharma

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 6
  • Latest Approval Date Dec 30, 1991
  • Data Source FDA
  • First Approval Date Dec 28, 1984
Company Overview

Company

Promius Pharma

Country

U.S.A

Website

Visit Website

Email

API@drreddys.com

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Company Snapshot

Promius Pharma

107 College Rd E Princeton, NJ 08540

U.S.A

api.drreddys.com/ API@drreddys.com View on Map
FDA Approved Drug Records ( 6 records )
1991
30 Dec
Discontinued Application: 19091

Drug Name

ISMO

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1991-12-30

19091 / 1

Active Ingredient

ISOSORBIDE MONONITRATE

Application Number

19091

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1991-12-30

Regulatory Status

Discontinued

1984
28 Dec
Discontinued Application: 18917

Drug Name

SECTRAL

Product Number

1

Dosage Form

-

Strength

EQ 200MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1984-12-28

18917 / 1

Active Ingredient

ACEBUTOLOL HYDROCHLORIDE

Application Number

18917

Product Number

1

Dosage Form

-

Strength

EQ 200MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1984-12-28

Regulatory Status

Discontinued

1984
28 Dec
Discontinued Application: 18917

Drug Name

SECTRAL

Product Number

3

Dosage Form

-

Strength

EQ 400MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1984-12-28

18917 / 3

Active Ingredient

ACEBUTOLOL HYDROCHLORIDE

Application Number

18917

Product Number

3

Dosage Form

-

Strength

EQ 400MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1984-12-28

Regulatory Status

Discontinued

1986
27 Oct
Discontinued Application: 19032

Drug Name

TENEX

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1986-10-27

19032 / 1

Active Ingredient

GUANFACINE HYDROCHLORIDE

Application Number

19032

Product Number

1

Dosage Form

-

Strength

EQ 1MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1986-10-27

Regulatory Status

Discontinued

1988
07 Nov
Discontinued Application: 19032

Drug Name

TENEX

Product Number

2

Dosage Form

-

Strength

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

Approval Date

1988-11-07

19032 / 2

Active Ingredient

GUANFACINE HYDROCHLORIDE

Application Number

19032

Product Number

2

Dosage Form

-

Strength

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

Approval Date

1988-11-07

Regulatory Status

Discontinued

1988
07 Nov
Discontinued Application: 19032

Drug Name

TENEX

Product Number

3

Dosage Form

-

Strength

EQ 3MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1988-11-07

19032 / 3

Active Ingredient

GUANFACINE HYDROCHLORIDE

Application Number

19032

Product Number

3

Dosage Form

-

Strength

EQ 3MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1988-11-07

Regulatory Status

Discontinued

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Drug Status Breakdown
6 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

ISMO

Application Number

19091

Product Number

1

Active Ingredient

ISOSORBIDE MONONITRATE

Dosage Form

-

Strength

20MG

FDA Approved Drug Data

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