VALIDUS PHARMS
FDA Approved Drugs

VALIDUS PHARMS

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 RX
  • Total Records 35
  • Latest Approval Date Dec 10, 2004
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
35
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Discontinued
20
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RX
15
View
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Company

VALIDUS PHARMS

Country

U.S.A

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VALIDUS PHARMS

U.S.A

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FDA Approved Drug Records ( 35 records )
1997
11 Sep
Discontinued Application: 20623

Drug Name

ANZEMET

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1997-09-11

20623 / 1

Active Ingredient

DOLASETRON MESYLATE

Application Number

20623

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1997-09-11

Regulatory Status

Discontinued

1997
11 Sep
Discontinued Application: 20623

Drug Name

ANZEMET

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

1997-09-11

20623 / 2

Active Ingredient

DOLASETRON MESYLATE

Application Number

20623

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

1997-09-11

Regulatory Status

Discontinued

1997
11 Sep
Discontinued Application: 20624

Drug Name

ANZEMET

Product Number

1

Dosage Form

-

Strength

100MG/5ML (20MG/ML)

Approval Date

1997-09-11

20624 / 1

Active Ingredient

DOLASETRON MESYLATE

Application Number

20624

Product Number

1

Dosage Form

-

Strength

100MG/5ML (20MG/ML)

Approval Date

1997-09-11

Regulatory Status

Discontinued

1997
11 Sep
Discontinued Application: 20624

Drug Name

ANZEMET

Product Number

2

Dosage Form

-

Strength

12.5MG/0.625ML (20MG/ML)

Approval Date

1997-09-11

20624 / 2

Active Ingredient

DOLASETRON MESYLATE

Application Number

20624

Product Number

2

Dosage Form

-

Strength

12.5MG/0.625ML (20MG/ML)

Approval Date

1997-09-11

Regulatory Status

Discontinued

2001
11 Dec
Discontinued Application: 20624

Drug Name

ANZEMET

Product Number

3

Dosage Form

-

Strength

500MG/25ML (20MG/ML)

Approval Date

2001-12-11

20624 / 3

Active Ingredient

DOLASETRON MESYLATE

Application Number

20624

Product Number

3

Dosage Form

-

Strength

500MG/25ML (20MG/ML)

Approval Date

2001-12-11

Regulatory Status

Discontinued

1983
28 Feb
RX Application: 18225

Drug Name

BUMEX

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1983-02-28

18225 / 1

Active Ingredient

BUMETANIDE

Application Number

18225

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1983-02-28

Regulatory Status

RX

1983
28 Feb
RX Application: 18225

Drug Name

BUMEX

Product Number

2

Dosage Form

-

Strength

0.5MG

Approval Date

1983-02-28

18225 / 2

Active Ingredient

BUMETANIDE

Application Number

18225

Product Number

2

Dosage Form

-

Strength

0.5MG

Approval Date

1983-02-28

Regulatory Status

RX

1985
14 Jun
RX Application: 18225

Drug Name

BUMEX

Product Number

3

Dosage Form

-

Strength

2MG

Approval Date

1985-06-14

18225 / 3

Active Ingredient

BUMETANIDE

Application Number

18225

Product Number

3

Dosage Form

-

Strength

2MG

Approval Date

1985-06-14

Regulatory Status

RX

1983
28 Feb
Discontinued Application: 18226

Drug Name

BUMEX

Product Number

1

Dosage Form

-

Strength

0.25MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1983-02-28

18226 / 1

Active Ingredient

BUMETANIDE

Application Number

18226

Product Number

1

Dosage Form

-

Strength

0.25MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1983-02-28

Regulatory Status

Discontinued

2004
10 Dec
RX Application: 21710

Drug Name

EQUETRO

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2004-12-10

21710 / 1

Active Ingredient

CARBAMAZEPINE

Application Number

21710

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

2004-12-10

Regulatory Status

RX

2004
10 Dec
RX Application: 21710

Drug Name

EQUETRO

Product Number

2

Dosage Form

-

Strength

200MG

Approval Date

2004-12-10

21710 / 2

Active Ingredient

CARBAMAZEPINE

Application Number

21710

Product Number

2

Dosage Form

-

Strength

200MG

Approval Date

2004-12-10

Regulatory Status

RX

2004
10 Dec
RX Application: 21710

Drug Name

EQUETRO

Product Number

3

Dosage Form

-

Strength

300MG

Approval Date

2004-12-10

21710 / 3

Active Ingredient

CARBAMAZEPINE

Application Number

21710

Product Number

3

Dosage Form

-

Strength

300MG

Approval Date

2004-12-10

Regulatory Status

RX

1982
01 Jan
Discontinued Application: 16273

Drug Name

LASIX

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-01-01

16273 / 1

Active Ingredient

FUROSEMIDE

Application Number

16273

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 16273

Drug Name

LASIX

Product Number

2

Dosage Form

-

Strength

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

Approval Date

1982-01-01

16273 / 2

Active Ingredient

FUROSEMIDE

Application Number

16273

Product Number

2

Dosage Form

-

Strength

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

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 16273

Drug Name

LASIX

Product Number

3

Dosage Form

-

Strength

80MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

16273 / 3

Active Ingredient

FUROSEMIDE

Application Number

16273

Product Number

3

Dosage Form

-

Strength

80MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
RX Application: 17963

Drug Name

LOPRESSOR

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

17963 / 1

Active Ingredient

METOPROLOL TARTRATE

Application Number

17963

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

RX

1982
01 Jan
RX Application: 17963

Drug Name

LOPRESSOR

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

17963 / 2

Active Ingredient

METOPROLOL TARTRATE

Application Number

17963

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

RX

1984
31 Dec
RX Application: 18303

Drug Name

LOPRESSOR HCT

Product Number

1

Dosage Form

-

Strength

25MG;50MG

Approval Date

1984-12-31

18303 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE; METOPROLOL TARTRATE

Application Number

18303

Product Number

1

Dosage Form

-

Strength

25MG;50MG

Approval Date

1984-12-31

Regulatory Status

RX

1984
31 Dec
Discontinued Application: 18303

Drug Name

LOPRESSOR HCT

Product Number

2

Dosage Form

-

Strength

25MG;100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1984-12-31

18303 / 2

Active Ingredient

HYDROCHLOROTHIAZIDE; METOPROLOL TARTRATE

Application Number

18303

Product Number

2

Dosage Form

-

Strength

25MG;100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1984-12-31

Regulatory Status

Discontinued

1984
31 Dec
Discontinued Application: 18303

Drug Name

LOPRESSOR HCT

Product Number

3

Dosage Form

-

Strength

50MG;100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1984-12-31

18303 / 3

Active Ingredient

HYDROCHLOROTHIAZIDE; METOPROLOL TARTRATE

Application Number

18303

Product Number

3

Dosage Form

-

Strength

50MG;100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1984-12-31

Regulatory Status

Discontinued

1991
25 Jun
Discontinued Application: 19851

Drug Name

LOTENSIN

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1991-06-25

19851 / 1

Active Ingredient

BENAZEPRIL HYDROCHLORIDE

Application Number

19851

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1991-06-25

Regulatory Status

Discontinued

1991
25 Jun
RX Application: 19851

Drug Name

LOTENSIN

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

1991-06-25

19851 / 2

Active Ingredient

BENAZEPRIL HYDROCHLORIDE

Application Number

19851

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

1991-06-25

Regulatory Status

RX

1991
25 Jun
RX Application: 19851

Drug Name

LOTENSIN

Product Number

3

Dosage Form

-

Strength

20MG

Approval Date

1991-06-25

19851 / 3

Active Ingredient

BENAZEPRIL HYDROCHLORIDE

Application Number

19851

Product Number

3

Dosage Form

-

Strength

20MG

Approval Date

1991-06-25

Regulatory Status

RX

1991
25 Jun
RX Application: 19851

Drug Name

LOTENSIN

Product Number

4

Dosage Form

-

Strength

40MG

Approval Date

1991-06-25

19851 / 4

Active Ingredient

BENAZEPRIL HYDROCHLORIDE

Application Number

19851

Product Number

4

Dosage Form

-

Strength

40MG

Approval Date

1991-06-25

Regulatory Status

RX

1992
19 May
Discontinued Application: 20033

Drug Name

LOTENSIN HCT

Product Number

1

Dosage Form

-

Strength

5MG;6.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1992-05-19

20033 / 1

Active Ingredient

BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE

Application Number

20033

Product Number

1

Dosage Form

-

Strength

5MG;6.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1992-05-19

Regulatory Status

Discontinued

1992
19 May
RX Application: 20033

Drug Name

LOTENSIN HCT

Product Number

2

Dosage Form

-

Strength

10MG;12.5MG

Approval Date

1992-05-19

20033 / 2

Active Ingredient

BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE

Application Number

20033

Product Number

2

Dosage Form

-

Strength

10MG;12.5MG

Approval Date

1992-05-19

Regulatory Status

RX

1992
19 May
RX Application: 20033

Drug Name

LOTENSIN HCT

Product Number

3

Dosage Form

-

Strength

20MG;25MG

Approval Date

1992-05-19

20033 / 3

Active Ingredient

BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE

Application Number

20033

Product Number

3

Dosage Form

-

Strength

20MG;25MG

Approval Date

1992-05-19

Regulatory Status

RX

1992
19 May
RX Application: 20033

Drug Name

LOTENSIN HCT

Product Number

4

Dosage Form

-

Strength

20MG;12.5MG

Approval Date

1992-05-19

20033 / 4

Active Ingredient

BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE

Application Number

20033

Product Number

4

Dosage Form

-

Strength

20MG;12.5MG

Approval Date

1992-05-19

Regulatory Status

RX

1982
01 Jan
Discontinued Application: 14399

Drug Name

NORPRAMIN

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

14399 / 1

Active Ingredient

DESIPRAMINE HYDROCHLORIDE

Application Number

14399

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 14399

Drug Name

NORPRAMIN

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

14399 / 3

Active Ingredient

DESIPRAMINE HYDROCHLORIDE

Application Number

14399

Product Number

3

Dosage Form

-

Strength

50MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 14399

Drug Name

NORPRAMIN

Product Number

4

Dosage Form

-

Strength

75MG

Approval Date

1982-01-01

14399 / 4

Active Ingredient

DESIPRAMINE HYDROCHLORIDE

Application Number

14399

Product Number

4

Dosage Form

-

Strength

75MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 14399

Drug Name

NORPRAMIN

Product Number

5

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

14399 / 5

Active Ingredient

DESIPRAMINE HYDROCHLORIDE

Application Number

14399

Product Number

5

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 14399

Drug Name

NORPRAMIN

Product Number

6

Dosage Form

-

Strength

150MG

Approval Date

1982-01-01

14399 / 6

Active Ingredient

DESIPRAMINE HYDROCHLORIDE

Application Number

14399

Product Number

6

Dosage Form

-

Strength

150MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
11 Feb
Discontinued Application: 14399

Drug Name

NORPRAMIN

Product Number

7

Dosage Form

-

Strength

10MG

Approval Date

1982-02-11

14399 / 7

Active Ingredient

DESIPRAMINE HYDROCHLORIDE

Application Number

14399

Product Number

7

Dosage Form

-

Strength

10MG

Approval Date

1982-02-11

Regulatory Status

Discontinued

1984
30 Aug
Discontinued Application: 18631

Drug Name

TRENTAL

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1984-08-30

18631 / 1

Active Ingredient

PENTOXIFYLLINE

Application Number

18631

Product Number

1

Dosage Form

-

Strength

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

Approval Date

1984-08-30

Regulatory Status

Discontinued

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Drug Status Breakdown
35 total
  • Discontinued
  • 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

ANZEMET

Application Number

20623

Product Number

1

Active Ingredient

DOLASETRON MESYLATE

Dosage Form

-

Strength

50MG

FDA Approved Drug Data

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