VALIDUS PHARMS RX
FDA Approved Drugs

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

Company

VALIDUS PHARMS RX

Country

U.S.A

Website

Email

Social Profiles

Company Snapshot

VALIDUS PHARMS RX

U.S.A

View on Map
FDA Approved Drug Records ( 15 records )
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

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
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

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
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

Related Databases
  • FDA Inspections
    0 View
  • EDQM CEP
    0 View
  • KDMF
    0 View
  • Japan DMF
    0 View
  • Eudra GMP
    0 View
  • NDC Database
    0 View
  • FDA Approved Drugs Database
    35 View
  • Drug Prices in Switzerland
    0 View
Drug Status Breakdown
15 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

BUMEX

Application Number

18225

Product Number

1

Active Ingredient

BUMETANIDE

Dosage Form

-

Strength

1MG

FDA Approved Drug Data

Approved drug product information

Regular Updates

Data maintained from official sources

Structured Database

Searchable pharmaceutical data

Reliable Data

Organized FDA drug records

Create a New Buying Request

Fields marked with * are mandatory.

Please enter quantity.
Please select a unit.
Please select quality standard.
Please select request type.
Please provide product specifications.
Please enter additional details.
Please select shipping preference.
Notice: By submitting this buying request, the provided product details and requirements may be published publicly on our marketplace.
Login to Submit