Salix Pharmaceuticals Discontinued
FDA Approved Drugs

Salix Pharmaceuticals 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 18
  • Latest Approval Date Dec 04, 2009
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
30
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Discontinued
18
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RX
12
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Company Overview

Company

Salix Pharmaceuticals Discontinued

Country

U.S.A

Website

Visit Website

Email

Salixmc@dlss.com

Social Profiles

LinkedIn
Company Snapshot

Salix Pharmaceuticals Discontinued

400 Somerset Corporate Blvd. Bridgewater, NJ 08807 USA

U.S.A

www.salix.com/ Salixmc@dlss.com View on Map
FDA Approved Drug Records ( 18 records )
1982
01 Jan
Discontinued Application: 11870

Drug Name

DIURIL

Product Number

1

Dosage Form

-

Strength

250MG/5ML

Approval Date

1982-01-01

11870 / 1

Active Ingredient

CHLOROTHIAZIDE

Application Number

11870

Product Number

1

Dosage Form

-

Strength

250MG/5ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

2007
10 Aug
Discontinued Application: 22118

Drug Name

FENOGLIDE

Product Number

1

Dosage Form

-

Strength

40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2007-08-10

22118 / 1

Active Ingredient

FENOFIBRATE

Application Number

22118

Product Number

1

Dosage Form

-

Strength

40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2007-08-10

Regulatory Status

Discontinued

2007
10 Aug
Discontinued Application: 22118

Drug Name

FENOGLIDE

Product Number

2

Dosage Form

-

Strength

120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2007-08-10

22118 / 2

Active Ingredient

FENOFIBRATE

Application Number

22118

Product Number

2

Dosage Form

-

Strength

120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2007-08-10

Regulatory Status

Discontinued

2005
03 Jun
Discontinued Application: 21748

Drug Name

GLUMETZA

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2005-06-03

21748 / 1

Active Ingredient

METFORMIN HYDROCHLORIDE

Application Number

21748

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2005-06-03

Regulatory Status

Discontinued

2005
03 Jun
Discontinued Application: 21748

Drug Name

GLUMETZA

Product Number

2

Dosage Form

-

Strength

1GM

Approval Date

2005-06-03

21748 / 2

Active Ingredient

METFORMIN HYDROCHLORIDE

Application Number

21748

Product Number

2

Dosage Form

-

Strength

1GM

Approval Date

2005-06-03

Regulatory Status

Discontinued

2009
04 Dec
Discontinued Application: 22456

Drug Name

MAGNESIUM HYDROXIDE AND OMEPRAZOLE AND SODIUM BICARBONATE

Product Number

1

Dosage Form

-

Strength

343MG;20MG;750MG

Approval Date

2009-12-04

22456 / 1

Active Ingredient

MAGNESIUM HYDROXIDE; OMEPRAZOLE; SODIUM BICARBONATE

Application Number

22456

Product Number

1

Dosage Form

-

Strength

343MG;20MG;750MG

Approval Date

2009-12-04

Regulatory Status

Discontinued

2009
04 Dec
Discontinued Application: 22456

Drug Name

MAGNESIUM HYDROXIDE AND OMEPRAZOLE AND SODIUM BICARBONATE

Product Number

2

Dosage Form

-

Strength

343MG;40MG;750MG

Approval Date

2009-12-04

22456 / 2

Active Ingredient

MAGNESIUM HYDROXIDE; OMEPRAZOLE; SODIUM BICARBONATE

Application Number

22456

Product Number

2

Dosage Form

-

Strength

343MG;40MG;750MG

Approval Date

2009-12-04

Regulatory Status

Discontinued

2009
04 Sep
Discontinued Application: 22246

Drug Name

METOZOLV ODT

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2009-09-04

22246 / 1

Active Ingredient

METOCLOPRAMIDE HYDROCHLORIDE

Application Number

22246

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2009-09-04

Regulatory Status

Discontinued

2009
04 Sep
Discontinued Application: 22246

Drug Name

METOZOLV ODT

Product Number

2

Dosage Form

-

Strength

EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2009-09-04

22246 / 2

Active Ingredient

METOCLOPRAMIDE HYDROCHLORIDE

Application Number

22246

Product Number

2

Dosage Form

-

Strength

EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2009-09-04

Regulatory Status

Discontinued

2006
16 Mar
Discontinued Application: 21892

Drug Name

OSMOPREP

Product Number

1

Dosage Form

-

Strength

0.398GM;1.102GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2006-03-16

21892 / 1

Active Ingredient

SODIUM PHOSPHATE, DIBASIC, ANHYDROUS; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE

Application Number

21892

Product Number

1

Dosage Form

-

Strength

0.398GM;1.102GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2006-03-16

Regulatory Status

Discontinued

1987
02 Feb
Discontinued Application: 19527

Drug Name

PEPCID

Product Number

1

Dosage Form

-

Strength

40MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1987-02-02

19527 / 1

Active Ingredient

FAMOTIDINE

Application Number

19527

Product Number

1

Dosage Form

-

Strength

40MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1987-02-02

Regulatory Status

Discontinued

2000
21 Sep
Discontinued Application: 21097

Drug Name

VISICOL

Product Number

1

Dosage Form

-

Strength

0.398GM;1.102GM

Approval Date

2000-09-21

21097 / 1

Active Ingredient

SODIUM PHOSPHATE, DIBASIC, ANHYDROUS; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE

Application Number

21097

Product Number

1

Dosage Form

-

Strength

0.398GM;1.102GM

Approval Date

2000-09-21

Regulatory Status

Discontinued

2004
15 Jun
Discontinued Application: 21636

Drug Name

ZEGERID

Product Number

1

Dosage Form

-

Strength

20MG/PACKET;1.68GM/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2004-06-15

21636 / 1

Active Ingredient

OMEPRAZOLE; SODIUM BICARBONATE

Application Number

21636

Product Number

1

Dosage Form

-

Strength

20MG/PACKET;1.68GM/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2004-06-15

Regulatory Status

Discontinued

2004
21 Dec
Discontinued Application: 21636

Drug Name

ZEGERID

Product Number

2

Dosage Form

-

Strength

40MG/PACKET;1.68GM/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2004-12-21

21636 / 2

Active Ingredient

OMEPRAZOLE; SODIUM BICARBONATE

Application Number

21636

Product Number

2

Dosage Form

-

Strength

40MG/PACKET;1.68GM/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2004-12-21

Regulatory Status

Discontinued

2006
27 Feb
Discontinued Application: 21849

Drug Name

ZEGERID

Product Number

1

Dosage Form

-

Strength

20MG;1.1GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2006-02-27

21849 / 1

Active Ingredient

OMEPRAZOLE; SODIUM BICARBONATE

Application Number

21849

Product Number

1

Dosage Form

-

Strength

20MG;1.1GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2006-02-27

Regulatory Status

Discontinued

2006
27 Feb
Discontinued Application: 21849

Drug Name

ZEGERID

Product Number

2

Dosage Form

-

Strength

40MG;1.1GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2006-02-27

21849 / 2

Active Ingredient

OMEPRAZOLE; SODIUM BICARBONATE

Application Number

21849

Product Number

2

Dosage Form

-

Strength

40MG;1.1GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2006-02-27

Regulatory Status

Discontinued

2006
24 Mar
Discontinued Application: 21850

Drug Name

ZEGERID

Product Number

1

Dosage Form

-

Strength

700MG;20MG;600MG

Approval Date

2006-03-24

21850 / 1

Active Ingredient

MAGNESIUM HYDROXIDE; OMEPRAZOLE; SODIUM BICARBONATE

Application Number

21850

Product Number

1

Dosage Form

-

Strength

700MG;20MG;600MG

Approval Date

2006-03-24

Regulatory Status

Discontinued

2006
24 Mar
Discontinued Application: 21850

Drug Name

ZEGERID

Product Number

2

Dosage Form

-

Strength

700MG;40MG;600MG

Approval Date

2006-03-24

21850 / 2

Active Ingredient

MAGNESIUM HYDROXIDE; OMEPRAZOLE; SODIUM BICARBONATE

Application Number

21850

Product Number

2

Dosage Form

-

Strength

700MG;40MG;600MG

Approval Date

2006-03-24

Regulatory Status

Discontinued

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Drug Status Breakdown
18 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

DIURIL

Application Number

11870

Product Number

1

Active Ingredient

CHLOROTHIAZIDE

Dosage Form

-

Strength

250MG/5ML

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