CYPRESS PHARM
FDA Approved Drugs

CYPRESS PHARM

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 Aug 23, 2010
  • Data Source FDA
  • First Approval Date Oct 10, 2008
Company Overview

Company

CYPRESS PHARM

Country

U.S.A

Website

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Company Snapshot

CYPRESS PHARM

10 North Park Place, Suite 201, Morristown, NJ 07960

U.S.A

www.pernixtx.com/ View on Map
FDA Approved Drug Records ( 5 records )
2010
23 Aug
Discontinued Application: 90417

Drug Name

CARBINOXAMINE MALEATE

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

2010-08-23

90417 / 1

Active Ingredient

CARBINOXAMINE MALEATE

Application Number

90417

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

2010-08-23

Regulatory Status

Discontinued

2010
04 May
Discontinued Application: 90418

Drug Name

CARBINOXAMINE MALEATE

Product Number

1

Dosage Form

-

Strength

4MG/5ML

Approval Date

2010-05-04

90418 / 1

Active Ingredient

CARBINOXAMINE MALEATE

Application Number

90418

Product Number

1

Dosage Form

-

Strength

4MG/5ML

Approval Date

2010-05-04

Regulatory Status

Discontinued

2008
10 Oct
Discontinued Application: 90300

Drug Name

CHILDRENS CETIRIZINE HYDROCHLORIDE ALLERGY

Product Number

1

Dosage Form

-

Strength

5MG/5ML

Approval Date

2008-10-10

90300 / 1

Active Ingredient

CETIRIZINE HYDROCHLORIDE

Application Number

90300

Product Number

1

Dosage Form

-

Strength

5MG/5ML

Approval Date

2008-10-10

Regulatory Status

Discontinued

2008
10 Oct
Discontinued Application: 90300

Drug Name

CHILDRENS CETIRIZINE HYDROCHLORIDE HIVES RELIEF

Product Number

2

Dosage Form

-

Strength

5MG/5ML

Approval Date

2008-10-10

90300 / 2

Active Ingredient

CETIRIZINE HYDROCHLORIDE

Application Number

90300

Product Number

2

Dosage Form

-

Strength

5MG/5ML

Approval Date

2008-10-10

Regulatory Status

Discontinued

2008
25 Nov
Discontinued Application: 78502

Drug Name

ELIPHOS

Product Number

1

Dosage Form

-

Strength

667MG

Approval Date

2008-11-25

78502 / 1

Active Ingredient

CALCIUM ACETATE

Application Number

78502

Product Number

1

Dosage Form

-

Strength

667MG

Approval Date

2008-11-25

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

CARBINOXAMINE MALEATE

Application Number

90417

Product Number

1

Active Ingredient

CARBINOXAMINE MALEATE

Dosage Form

-

Strength

4MG

FDA Approved Drug Data

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