BD RX INC
FDA Approved Drugs

BD RX INC

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.

OTC Discontinued
  • Total Records 5
  • Latest Approval Date Mar 14, 2000
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
5
View
Discontinued
4
View
OTC
1
View
Company Overview

Company

BD RX INC

Country

U.S.A

Email

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Company Snapshot

BD RX INC

BD Rx Inc., 1 Becton Drive, Franklin Lakes, NJ 07417

U.S.A

www.bdrxinc.com/ View on Map
FDA Approved Drug Records ( 5 records )
1989
24 Oct
OTC Application: 72525

Drug Name

CHLORHEXIDINE GLUCONATE

Product Number

1

Dosage Form

-

Strength

4%

Approval Date

1989-10-24

72525 / 1

Active Ingredient

CHLORHEXIDINE GLUCONATE

Application Number

72525

Product Number

1

Dosage Form

-

Strength

4%

Approval Date

1989-10-24

Regulatory Status

OTC

1982
01 Jan
Discontinued Application: 17452

Drug Name

E-Z SCRUB

Product Number

1

Dosage Form

-

Strength

450MG

Approval Date

1982-01-01

17452 / 1

Active Ingredient

HEXACHLOROPHENE

Application Number

17452

Product Number

1

Dosage Form

-

Strength

450MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

2000
14 Mar
Discontinued Application: 73416

Drug Name

E-Z SCRUB

Product Number

1

Dosage Form

-

Strength

4%

Approval Date

2000-03-14

73416 / 1

Active Ingredient

CHLORHEXIDINE GLUCONATE

Application Number

73416

Product Number

1

Dosage Form

-

Strength

4%

Approval Date

2000-03-14

Regulatory Status

Discontinued

1985
29 Nov
Discontinued Application: 19240

Drug Name

E-Z SCRUB 201

Product Number

1

Dosage Form

-

Strength

20%

Approval Date

1985-11-29

19240 / 1

Active Ingredient

POVIDONE-IODINE

Application Number

19240

Product Number

1

Dosage Form

-

Strength

20%

Approval Date

1985-11-29

Regulatory Status

Discontinued

1987
07 Jan
Discontinued Application: 19476

Drug Name

E-Z SCRUB 241

Product Number

1

Dosage Form

-

Strength

10%

Approval Date

1987-01-07

19476 / 1

Active Ingredient

POVIDONE-IODINE

Application Number

19476

Product Number

1

Dosage Form

-

Strength

10%

Approval Date

1987-01-07

Regulatory Status

Discontinued

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Drug Status Breakdown
5 total
  • OTC
  • 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

CHLORHEXIDINE GLUCONATE

Application Number

72525

Product Number

1

Active Ingredient

CHLORHEXIDINE GLUCONATE

Dosage Form

-

Strength

4%

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