Bracco RX
FDA Approved Drugs

Bracco 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 44
  • Latest Approval Date Aug 01, 2025
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
107
View
Unclassified
1
View
Discontinued
62
View
RX
44
View
Company Overview

Company

Bracco RX

Country

Italy

Website

Visit Website

Email

info@bracco.com

Social Profiles

LinkedIn
Company Snapshot

Bracco RX

Via Caduti di Marcinelle 13, 20134 Milan

Italy

www.bracco.com/en info@bracco.com View on Map
FDA Approved Drug Records ( 44 records )
1989
29 Dec
RX Application: 19414

Drug Name

CARDIOGEN-82

Product Number

1

Dosage Form

-

Strength

N/A

Approval Date

1989-12-29

19414 / 1

Active Ingredient

RUBIDIUM CHLORIDE RB-82

Application Number

19414

Product Number

1

Dosage Form

-

Strength

N/A

Approval Date

1989-12-29

Regulatory Status

RX

1987
21 Jan
RX Application: 18963

Drug Name

CHOLETEC

Product Number

1

Dosage Form

-

Strength

N/A

Approval Date

1987-01-21

18963 / 1

Active Ingredient

TECHNETIUM TC-99M MEBROFENIN KIT

Application Number

18963

Product Number

1

Dosage Form

-

Strength

N/A

Approval Date

1987-01-21

Regulatory Status

RX

1982
01 Jan
RX Application: 10040

Drug Name

CYSTOGRAFIN

Product Number

18

Dosage Form

-

Strength

30%

Approval Date

1982-01-01

10040 / 18

Active Ingredient

DIATRIZOATE MEGLUMINE

Application Number

10040

Product Number

18

Dosage Form

-

Strength

30%

Approval Date

1982-01-01

Regulatory Status

RX

1982
09 Nov
RX Application: 10040

Drug Name

CYSTOGRAFIN DILUTE

Product Number

22

Dosage Form

-

Strength

18%

Approval Date

1982-11-09

10040 / 22

Active Ingredient

DIATRIZOATE MEGLUMINE

Application Number

10040

Product Number

22

Dosage Form

-

Strength

18%

Approval Date

1982-11-09

Regulatory Status

RX

2025
01 Aug
RX Application: 219840

Drug Name

E-Z-DISK

Product Number

1

Dosage Form

-

Strength

700MG

Approval Date

2025-08-01

219840 / 1

Active Ingredient

BARIUM SULFATE

Application Number

219840

Product Number

1

Dosage Form

-

Strength

700MG

Approval Date

2025-08-01

Regulatory Status

RX

2016
11 Jan
RX Application: 208036

Drug Name

E-Z-HD

Product Number

1

Dosage Form

-

Strength

98%

Approval Date

2016-01-11

208036 / 1

Active Ingredient

BARIUM SULFATE

Application Number

208036

Product Number

1

Dosage Form

-

Strength

98%

Approval Date

2016-01-11

Regulatory Status

RX

2017
07 Apr
RX Application: 208036

Drug Name

E-Z-PAQUE

Product Number

2

Dosage Form

-

Strength

96%

Approval Date

2017-04-07

208036 / 2

Active Ingredient

BARIUM SULFATE

Application Number

208036

Product Number

2

Dosage Form

-

Strength

96%

Approval Date

2017-04-07

Regulatory Status

RX

2020
29 May
RX Application: 208143

Drug Name

ENTERO VU 24%

Product Number

8

Dosage Form

-

Strength

24%

Approval Date

2020-05-29

208143 / 8

Active Ingredient

BARIUM SULFATE

Application Number

208143

Product Number

8

Dosage Form

-

Strength

24%

Approval Date

2020-05-29

Regulatory Status

RX

1982
01 Jan
RX Application: 11245

Drug Name

GASTROGRAFIN

Product Number

3

Dosage Form

-

Strength

66%;10%

Approval Date

1982-01-01

11245 / 3

Active Ingredient

DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

Application Number

11245

Product Number

3

Dosage Form

-

Strength

66%;10%

Approval Date

1982-01-01

Regulatory Status

RX

2024
27 Nov
RX Application: 216016

Drug Name

IOMERVU

Product Number

7

Dosage Form

-

Strength

35GM IODINE/100ML (350MG IODINE/ML)

Approval Date

2024-11-27

216016 / 7

Active Ingredient

IOMEPROL

Application Number

216016

Product Number

7

Dosage Form

-

Strength

35GM IODINE/100ML (350MG IODINE/ML)

Approval Date

2024-11-27

Regulatory Status

RX

2024
27 Nov
RX Application: 216016

Drug Name

IOMERVU

Product Number

9

Dosage Form

-

Strength

70GM IODINE/200ML (350MG IODINE/ML)

Approval Date

2024-11-27

216016 / 9

Active Ingredient

IOMEPROL

Application Number

216016

Product Number

9

Dosage Form

-

Strength

70GM IODINE/200ML (350MG IODINE/ML)

Approval Date

2024-11-27

Regulatory Status

RX

2024
27 Nov
RX Application: 216016

Drug Name

IOMERVU

Product Number

11

Dosage Form

-

Strength

40GM IODINE/100ML (400MG IODINE/ML)

Approval Date

2024-11-27

216016 / 11

Active Ingredient

IOMEPROL

Application Number

216016

Product Number

11

Dosage Form

-

Strength

40GM IODINE/100ML (400MG IODINE/ML)

Approval Date

2024-11-27

Regulatory Status

RX

2024
27 Nov
RX Application: 216016

Drug Name

IOMERVU

Product Number

13

Dosage Form

-

Strength

80GM IODINE/200ML (400MG IODINE/ML)

Approval Date

2024-11-27

216016 / 13

Active Ingredient

IOMEPROL

Application Number

216016

Product Number

13

Dosage Form

-

Strength

80GM IODINE/200ML (400MG IODINE/ML)

Approval Date

2024-11-27

Regulatory Status

RX

2024
27 Nov
RX Application: 216017

Drug Name

IOMERVU

Product Number

7

Dosage Form

-

Strength

35GM IODINE/100ML (350MG IODINE/ML)

Approval Date

2024-11-27

216017 / 7

Active Ingredient

IOMEPROL

Application Number

216017

Product Number

7

Dosage Form

-

Strength

35GM IODINE/100ML (350MG IODINE/ML)

Approval Date

2024-11-27

Regulatory Status

RX

2024
27 Nov
RX Application: 216017

Drug Name

IOMERVU

Product Number

9

Dosage Form

-

Strength

70GM IODINE/200ML (350MG IODINE/ML)

Approval Date

2024-11-27

216017 / 9

Active Ingredient

IOMEPROL

Application Number

216017

Product Number

9

Dosage Form

-

Strength

70GM IODINE/200ML (350MG IODINE/ML)

Approval Date

2024-11-27

Regulatory Status

RX

2024
27 Nov
RX Application: 216017

Drug Name

IOMERVU

Product Number

11

Dosage Form

-

Strength

40GM IODINE/100ML (400MG IODINE/ML)

Approval Date

2024-11-27

216017 / 11

Active Ingredient

IOMEPROL

Application Number

216017

Product Number

11

Dosage Form

-

Strength

40GM IODINE/100ML (400MG IODINE/ML)

Approval Date

2024-11-27

Regulatory Status

RX

2024
27 Nov
RX Application: 216017

Drug Name

IOMERVU

Product Number

13

Dosage Form

-

Strength

80GM IODINE/200ML (400MG IODINE/ML)

Approval Date

2024-11-27

216017 / 13

Active Ingredient

IOMEPROL

Application Number

216017

Product Number

13

Dosage Form

-

Strength

80GM IODINE/200ML (400MG IODINE/ML)

Approval Date

2024-11-27

Regulatory Status

RX

1987
07 Jul
RX Application: 18735

Drug Name

ISOVUE-200

Product Number

6

Dosage Form

-

Strength

41%

Approval Date

1987-07-07

18735 / 6

Active Ingredient

IOPAMIDOL

Application Number

18735

Product Number

6

Dosage Form

-

Strength

41%

Approval Date

1987-07-07

Regulatory Status

RX

1992
06 Jul
RX Application: 18735

Drug Name

ISOVUE-250

Product Number

7

Dosage Form

-

Strength

51%

Approval Date

1992-07-06

18735 / 7

Active Ingredient

IOPAMIDOL

Application Number

18735

Product Number

7

Dosage Form

-

Strength

51%

Approval Date

1992-07-06

Regulatory Status

RX

1985
31 Dec
RX Application: 18735

Drug Name

ISOVUE-300

Product Number

2

Dosage Form

-

Strength

61%

Approval Date

1985-12-31

18735 / 2

Active Ingredient

IOPAMIDOL

Application Number

18735

Product Number

2

Dosage Form

-

Strength

61%

Approval Date

1985-12-31

Regulatory Status

RX

1994
12 Oct
RX Application: 20327

Drug Name

ISOVUE-300

Product Number

3

Dosage Form

-

Strength

61%

Approval Date

1994-10-12

20327 / 3

Active Ingredient

IOPAMIDOL

Application Number

20327

Product Number

3

Dosage Form

-

Strength

61%

Approval Date

1994-10-12

Regulatory Status

RX

1985
31 Dec
RX Application: 18735

Drug Name

ISOVUE-370

Product Number

3

Dosage Form

-

Strength

76%

Approval Date

1985-12-31

18735 / 3

Active Ingredient

IOPAMIDOL

Application Number

18735

Product Number

3

Dosage Form

-

Strength

76%

Approval Date

1985-12-31

Regulatory Status

RX

1994
12 Oct
RX Application: 20327

Drug Name

ISOVUE-370

Product Number

4

Dosage Form

-

Strength

76%

Approval Date

1994-10-12

20327 / 4

Active Ingredient

IOPAMIDOL

Application Number

20327

Product Number

4

Dosage Form

-

Strength

76%

Approval Date

1994-10-12

Regulatory Status

RX

1985
31 Dec
RX Application: 18735

Drug Name

ISOVUE-M 200

Product Number

1

Dosage Form

-

Strength

41%

Approval Date

1985-12-31

18735 / 1

Active Ingredient

IOPAMIDOL

Application Number

18735

Product Number

1

Dosage Form

-

Strength

41%

Approval Date

1985-12-31

Regulatory Status

RX

1985
31 Dec
RX Application: 18735

Drug Name

ISOVUE-M 300

Product Number

4

Dosage Form

-

Strength

61%

Approval Date

1985-12-31

18735 / 4

Active Ingredient

IOPAMIDOL

Application Number

18735

Product Number

4

Dosage Form

-

Strength

61%

Approval Date

1985-12-31

Regulatory Status

RX

1982
01 Jan
RX Application: 17697

Drug Name

KINEVAC

Product Number

1

Dosage Form

-

Strength

0.005MG/VIAL

Approval Date

1982-01-01

17697 / 1

Active Ingredient

SINCALIDE

Application Number

17697

Product Number

1

Dosage Form

-

Strength

0.005MG/VIAL

Approval Date

1982-01-01

Regulatory Status

RX

2017
01 Mar
RX Application: 208143

Drug Name

LIQUID E-Z-PAQUE

Product Number

3

Dosage Form

-

Strength

60%

Approval Date

2017-03-01

208143 / 3

Active Ingredient

BARIUM SULFATE

Application Number

208143

Product Number

3

Dosage Form

-

Strength

60%

Approval Date

2017-03-01

Regulatory Status

RX

2014
15 Oct
RX Application: 203684

Drug Name

LUMASON

Product Number

1

Dosage Form

-

Strength

60.7MG/25MG

Approval Date

2014-10-15

203684 / 1

Active Ingredient

SULFUR HEXAFLUORIDE LIPID-TYPE A MICROSPHERES

Application Number

203684

Product Number

1

Dosage Form

-

Strength

60.7MG/25MG

Approval Date

2014-10-15

Regulatory Status

RX

2004
23 Nov
RX Application: 21357

Drug Name

MULTIHANCE

Product Number

1

Dosage Form

-

Strength

2.645GM/5ML (529MG/ML)

Approval Date

2004-11-23

21357 / 1

Active Ingredient

GADOBENATE DIMEGLUMINE

Application Number

21357

Product Number

1

Dosage Form

-

Strength

2.645GM/5ML (529MG/ML)

Approval Date

2004-11-23

Regulatory Status

RX

2004
23 Nov
RX Application: 21357

Drug Name

MULTIHANCE

Product Number

2

Dosage Form

-

Strength

5.29GM/10ML (529MG/ML)

Approval Date

2004-11-23

21357 / 2

Active Ingredient

GADOBENATE DIMEGLUMINE

Application Number

21357

Product Number

2

Dosage Form

-

Strength

5.29GM/10ML (529MG/ML)

Approval Date

2004-11-23

Regulatory Status

RX

2004
23 Nov
RX Application: 21357

Drug Name

MULTIHANCE

Product Number

3

Dosage Form

-

Strength

7.935GM/15ML (529MG/ML)

Approval Date

2004-11-23

21357 / 3

Active Ingredient

GADOBENATE DIMEGLUMINE

Application Number

21357

Product Number

3

Dosage Form

-

Strength

7.935GM/15ML (529MG/ML)

Approval Date

2004-11-23

Regulatory Status

RX

2004
23 Nov
RX Application: 21357

Drug Name

MULTIHANCE

Product Number

4

Dosage Form

-

Strength

10.58GM/20ML (529MG/ML)

Approval Date

2004-11-23

21357 / 4

Active Ingredient

GADOBENATE DIMEGLUMINE

Application Number

21357

Product Number

4

Dosage Form

-

Strength

10.58GM/20ML (529MG/ML)

Approval Date

2004-11-23

Regulatory Status

RX

2004
23 Nov
RX Application: 21358

Drug Name

MULTIHANCE MULTIPACK

Product Number

1

Dosage Form

-

Strength

26.45GM/50ML (529MG/ML)

Approval Date

2004-11-23

21358 / 1

Active Ingredient

GADOBENATE DIMEGLUMINE

Application Number

21358

Product Number

1

Dosage Form

-

Strength

26.45GM/50ML (529MG/ML)

Approval Date

2004-11-23

Regulatory Status

RX

2004
23 Nov
RX Application: 21358

Drug Name

MULTIHANCE MULTIPACK

Product Number

2

Dosage Form

-

Strength

52.9GM/100ML (529MG/ML)

Approval Date

2004-11-23

21358 / 2

Active Ingredient

GADOBENATE DIMEGLUMINE

Application Number

21358

Product Number

2

Dosage Form

-

Strength

52.9GM/100ML (529MG/ML)

Approval Date

2004-11-23

Regulatory Status

RX

1992
16 Nov
RX Application: 20131

Drug Name

PROHANCE

Product Number

1

Dosage Form

-

Strength

279.3MG/ML

Approval Date

1992-11-16

20131 / 1

Active Ingredient

GADOTERIDOL

Application Number

20131

Product Number

1

Dosage Form

-

Strength

279.3MG/ML

Approval Date

1992-11-16

Regulatory Status

RX

2003
09 Oct
RX Application: 21489

Drug Name

PROHANCE MULTIPACK

Product Number

1

Dosage Form

-

Strength

279.3MG/ML

Approval Date

2003-10-09

21489 / 1

Active Ingredient

GADOTERIDOL

Application Number

21489

Product Number

1

Dosage Form

-

Strength

279.3MG/ML

Approval Date

2003-10-09

Regulatory Status

RX

2016
15 Jan
RX Application: 208143

Drug Name

READI-CAT 2

Product Number

1

Dosage Form

-

Strength

2%

Approval Date

2016-01-15

208143 / 1

Active Ingredient

BARIUM SULFATE

Application Number

208143

Product Number

1

Dosage Form

-

Strength

2%

Approval Date

2016-01-15

Regulatory Status

RX

2016
15 Jan
RX Application: 208143

Drug Name

READI-CAT 2 SMOOTHIE

Product Number

2

Dosage Form

-

Strength

2%

Approval Date

2016-01-15

208143 / 2

Active Ingredient

BARIUM SULFATE

Application Number

208143

Product Number

2

Dosage Form

-

Strength

2%

Approval Date

2016-01-15

Regulatory Status

RX

2017
04 Aug
RX Application: 208143

Drug Name

TAGITOL V

Product Number

5

Dosage Form

-

Strength

40%

Approval Date

2017-08-04

208143 / 5

Active Ingredient

BARIUM SULFATE

Application Number

208143

Product Number

5

Dosage Form

-

Strength

40%

Approval Date

2017-08-04

Regulatory Status

RX

2018
26 Mar
RX Application: 208143

Drug Name

VARIBAR HONEY

Product Number

7

Dosage Form

-

Strength

40%

Approval Date

2018-03-26

208143 / 7

Active Ingredient

BARIUM SULFATE

Application Number

208143

Product Number

7

Dosage Form

-

Strength

40%

Approval Date

2018-03-26

Regulatory Status

RX

2017
07 Jul
RX Application: 208143

Drug Name

VARIBAR NECTAR

Product Number

4

Dosage Form

-

Strength

40%

Approval Date

2017-07-07

208143 / 4

Active Ingredient

BARIUM SULFATE

Application Number

208143

Product Number

4

Dosage Form

-

Strength

40%

Approval Date

2017-07-07

Regulatory Status

RX

2016
14 Oct
RX Application: 208844

Drug Name

VARIBAR PUDDING

Product Number

1

Dosage Form

-

Strength

40%

Approval Date

2016-10-14

208844 / 1

Active Ingredient

BARIUM SULFATE

Application Number

208844

Product Number

1

Dosage Form

-

Strength

40%

Approval Date

2016-10-14

Regulatory Status

RX

2018
23 Jan
RX Application: 208143

Drug Name

VARIBAR THIN HONEY

Product Number

6

Dosage Form

-

Strength

40%

Approval Date

2018-01-23

208143 / 6

Active Ingredient

BARIUM SULFATE

Application Number

208143

Product Number

6

Dosage Form

-

Strength

40%

Approval Date

2018-01-23

Regulatory Status

RX

2019
30 Apr
RX Application: 208036

Drug Name

VARIBAR THIN LIQUID

Product Number

4

Dosage Form

-

Strength

81%

Approval Date

2019-04-30

208036 / 4

Active Ingredient

BARIUM SULFATE

Application Number

208036

Product Number

4

Dosage Form

-

Strength

81%

Approval Date

2019-04-30

Regulatory Status

RX

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Drug Status Breakdown
44 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

CARDIOGEN-82

Application Number

19414

Product Number

1

Active Ingredient

RUBIDIUM CHLORIDE RB-82

Dosage Form

-

Strength

N/A

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

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