IVAX Pharmaceuticals Inc RX
FDA Approved Drugs

IVAX Pharmaceuticals Inc RX

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
  • Total Records 33
  • Latest Approval Date Sep 19, 2024
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
326
View
Unclassified
3
View
Discontinued
289
View
OTC
1
View
RX
33
View
Company Overview

Company

IVAX Pharmaceuticals Inc RX

Country

U.S.A

Website

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Company Snapshot

IVAX Pharmaceuticals Inc RX

4400 Biscayne Blvd, Miami, FL 33137

U.S.A

www.tevapharm.com/ View on Map
FDA Approved Drug Records ( 33 records )
1988
21 Jul
RX Application: 72234

Drug Name

BACLOFEN

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1988-07-21

72234 / 1

Active Ingredient

BACLOFEN

Application Number

72234

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1988-07-21

Regulatory Status

RX

1988
21 Jul
RX Application: 72235

Drug Name

BACLOFEN

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1988-07-21

72235 / 1

Active Ingredient

BACLOFEN

Application Number

72235

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

1988-07-21

Regulatory Status

RX

2007
07 Mar
RX Application: 77750

Drug Name

CABERGOLINE

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

2007-03-07

77750 / 1

Active Ingredient

CABERGOLINE

Application Number

77750

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

2007-03-07

Regulatory Status

RX

2004
09 Jun
RX Application: 76089

Drug Name

CIPROFLOXACIN HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

2004-06-09

76089 / 2

Active Ingredient

CIPROFLOXACIN HYDROCHLORIDE

Application Number

76089

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

2004-06-09

Regulatory Status

RX

2004
09 Jun
RX Application: 76089

Drug Name

CIPROFLOXACIN HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

2004-06-09

76089 / 3

Active Ingredient

CIPROFLOXACIN HYDROCHLORIDE

Application Number

76089

Product Number

3

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

2004-06-09

Regulatory Status

RX

2004
09 Jun
RX Application: 76089

Drug Name

CIPROFLOXACIN HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

EQ 750MG BASE

Approval Date

2004-06-09

76089 / 4

Active Ingredient

CIPROFLOXACIN HYDROCHLORIDE

Application Number

76089

Product Number

4

Dosage Form

-

Strength

EQ 750MG BASE

Approval Date

2004-06-09

Regulatory Status

RX

1997
26 Nov
RX Application: 74949

Drug Name

CLOZAPINE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1997-11-26

74949 / 1

Active Ingredient

CLOZAPINE

Application Number

74949

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1997-11-26

Regulatory Status

RX

1997
26 Nov
RX Application: 74949

Drug Name

CLOZAPINE

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

1997-11-26

74949 / 2

Active Ingredient

CLOZAPINE

Application Number

74949

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

1997-11-26

Regulatory Status

RX

2003
31 Jul
RX Application: 74949

Drug Name

CLOZAPINE

Product Number

3

Dosage Form

-

Strength

12.5MG

Approval Date

2003-07-31

74949 / 3

Active Ingredient

CLOZAPINE

Application Number

74949

Product Number

3

Dosage Form

-

Strength

12.5MG

Approval Date

2003-07-31

Regulatory Status

RX

2005
25 Apr
RX Application: 74949

Drug Name

CLOZAPINE

Product Number

4

Dosage Form

-

Strength

50MG

Approval Date

2005-04-25

74949 / 4

Active Ingredient

CLOZAPINE

Application Number

74949

Product Number

4

Dosage Form

-

Strength

50MG

Approval Date

2005-04-25

Regulatory Status

RX

2005
16 Dec
RX Application: 76809

Drug Name

CLOZAPINE

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

2005-12-16

76809 / 1

Active Ingredient

CLOZAPINE

Application Number

76809

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

2005-12-16

Regulatory Status

RX

2005
16 Dec
RX Application: 76809

Drug Name

CLOZAPINE

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

2005-12-16

76809 / 2

Active Ingredient

CLOZAPINE

Application Number

76809

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

2005-12-16

Regulatory Status

RX

2005
16 Dec
RX Application: 76809

Drug Name

CLOZAPINE

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

2005-12-16

76809 / 3

Active Ingredient

CLOZAPINE

Application Number

76809

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

2005-12-16

Regulatory Status

RX

2005
25 Mar
RX Application: 65078

Drug Name

CYCLOSPORINE

Product Number

1

Dosage Form

-

Strength

100MG/ML

Approval Date

2005-03-25

65078 / 1

Active Ingredient

CYCLOSPORINE

Application Number

65078

Product Number

1

Dosage Form

-

Strength

100MG/ML

Approval Date

2005-03-25

Regulatory Status

RX

2005
29 Mar
RX Application: 65110

Drug Name

CYCLOSPORINE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

2005-03-29

65110 / 1

Active Ingredient

CYCLOSPORINE

Application Number

65110

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

2005-03-29

Regulatory Status

RX

2005
29 Mar
RX Application: 65110

Drug Name

CYCLOSPORINE

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

2005-03-29

65110 / 2

Active Ingredient

CYCLOSPORINE

Application Number

65110

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

2005-03-29

Regulatory Status

RX

2005
29 Mar
RX Application: 65110

Drug Name

CYCLOSPORINE

Product Number

3

Dosage Form

-

Strength

25MG

Approval Date

2005-03-29

65110 / 3

Active Ingredient

CYCLOSPORINE

Application Number

65110

Product Number

3

Dosage Form

-

Strength

25MG

Approval Date

2005-03-29

Regulatory Status

RX

1986
10 Dec
RX Application: 71307

Drug Name

DIAZEPAM

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1986-12-10

71307 / 1

Active Ingredient

DIAZEPAM

Application Number

71307

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1986-12-10

Regulatory Status

RX

1986
10 Dec
RX Application: 71321

Drug Name

DIAZEPAM

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1986-12-10

71321 / 1

Active Ingredient

DIAZEPAM

Application Number

71321

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1986-12-10

Regulatory Status

RX

1986
10 Dec
RX Application: 71322

Drug Name

DIAZEPAM

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1986-12-10

71322 / 1

Active Ingredient

DIAZEPAM

Application Number

71322

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1986-12-10

Regulatory Status

RX

2001
16 Apr
RX Application: 75511

Drug Name

FAMOTIDINE

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

2001-04-16

75511 / 1

Active Ingredient

FAMOTIDINE

Application Number

75511

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

2001-04-16

Regulatory Status

RX

2001
16 Apr
RX Application: 75511

Drug Name

FAMOTIDINE

Product Number

2

Dosage Form

-

Strength

40MG

Approval Date

2001-04-16

75511 / 2

Active Ingredient

FAMOTIDINE

Application Number

75511

Product Number

2

Dosage Form

-

Strength

40MG

Approval Date

2001-04-16

Regulatory Status

RX

2002
31 Jan
RX Application: 75245

Drug Name

FLUOXETINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2002-01-31

75245 / 1

Active Ingredient

FLUOXETINE HYDROCHLORIDE

Application Number

75245

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2002-01-31

Regulatory Status

RX

2002
31 Jan
RX Application: 75245

Drug Name

FLUOXETINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2002-01-31

75245 / 2

Active Ingredient

FLUOXETINE HYDROCHLORIDE

Application Number

75245

Product Number

2

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2002-01-31

Regulatory Status

RX

2004
28 Sep
RX Application: 75245

Drug Name

FLUOXETINE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2004-09-28

75245 / 3

Active Ingredient

FLUOXETINE HYDROCHLORIDE

Application Number

75245

Product Number

3

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2004-09-28

Regulatory Status

RX

2004
28 Apr
RX Application: 76017

Drug Name

GABAPENTIN

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2004-04-28

76017 / 1

Active Ingredient

GABAPENTIN

Application Number

76017

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2004-04-28

Regulatory Status

RX

2004
28 Apr
RX Application: 76017

Drug Name

GABAPENTIN

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

2004-04-28

76017 / 2

Active Ingredient

GABAPENTIN

Application Number

76017

Product Number

2

Dosage Form

-

Strength

300MG

Approval Date

2004-04-28

Regulatory Status

RX

2004
28 Apr
RX Application: 76017

Drug Name

GABAPENTIN

Product Number

3

Dosage Form

-

Strength

400MG

Approval Date

2004-04-28

76017 / 3

Active Ingredient

GABAPENTIN

Application Number

76017

Product Number

3

Dosage Form

-

Strength

400MG

Approval Date

2004-04-28

Regulatory Status

RX

1982
01 Jan
RX Application: 83177

Drug Name

HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

83177 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE

Application Number

83177

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

RX

1982
01 Jan
RX Application: 83177

Drug Name

HYDROCHLOROTHIAZIDE

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

83177 / 2

Active Ingredient

HYDROCHLOROTHIAZIDE

Application Number

83177

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

RX

2024
19 Sep
RX Application: 83177

Drug Name

HYDROCHLOROTHIAZIDE

Product Number

3

Dosage Form

-

Strength

12.5MG

Approval Date

2024-09-19

83177 / 3

Active Ingredient

HYDROCHLOROTHIAZIDE

Application Number

83177

Product Number

3

Dosage Form

-

Strength

12.5MG

Approval Date

2024-09-19

Regulatory Status

RX

2015
23 Feb
RX Application: 77006

Drug Name

TOLTERODINE TARTRATE

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

2015-02-23

77006 / 1

Active Ingredient

TOLTERODINE TARTRATE

Application Number

77006

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

2015-02-23

Regulatory Status

RX

2015
23 Feb
RX Application: 77006

Drug Name

TOLTERODINE TARTRATE

Product Number

2

Dosage Form

-

Strength

2MG

Approval Date

2015-02-23

77006 / 2

Active Ingredient

TOLTERODINE TARTRATE

Application Number

77006

Product Number

2

Dosage Form

-

Strength

2MG

Approval Date

2015-02-23

Regulatory Status

RX

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Drug Status Breakdown
33 total
  • RX
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

BACLOFEN

Application Number

72234

Product Number

1

Active Ingredient

BACLOFEN

Dosage Form

-

Strength

10MG

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

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