Jubilant DraxImage Inc
FDA Approved Drugs

Jubilant DraxImage 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.

Discontinued RX Unclassified
  • Total Records 9
  • Latest Approval Date Jan 30, 2023
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
9
View
Unclassified
2
View
Discontinued
3
View
RX
4
View
Company Overview

Company

Jubilant DraxImage Inc

Country

Canada

Website

Visit Website

Email

customerservice@jdi.jubl.com

Social Profiles

Company Snapshot

Jubilant DraxImage Inc

Jubilant DraxImage Inc.16751 TransCanada HighwayKirkland, Québec, CanadaH9H 4J4

Canada

www.draximage.com/en/home.html customerservice@jdi.jubl.com View on Map
FDA Approved Drug Records ( 9 records )
1982
01 Jan
Discontinued Application: 17714

Drug Name

AN-DTPA

Product Number

1

Dosage Form

-

Strength

N/A

Approval Date

1982-01-01

17714 / 1

Active Ingredient

TECHNETIUM TC-99M PENTETATE KIT

Application Number

17714

Product Number

1

Dosage Form

-

Strength

N/A

Approval Date

1982-01-01

Regulatory Status

Discontinued

2015
23 Jun
RX Application: 203920

Drug Name

FLUDEOXYGLUCOSE F18

Product Number

1

Dosage Form

-

Strength

20-300mCi/ML

Approval Date

2015-06-23

203920 / 1

Active Ingredient

FLUDEOXYGLUCOSE F-18

Application Number

203920

Product Number

1

Dosage Form

-

Strength

20-300mCi/ML

Approval Date

2015-06-23

Regulatory Status

RX

-
Unclassified Application: 17776

Drug Name

PULMOLITE

Product Number

1

Dosage Form

-

Strength

N/A

Approval Date

-

17776 / 1

Active Ingredient

TECHNETIUM TC-99M ALBUMIN AGGREGATED KIT

Application Number

17776

Product Number

1

Dosage Form

-

Strength

N/A

Approval Date

-

Regulatory Status

Unclassified

2015
23 Oct
RX Application: 203968

Drug Name

SODIUM FLUORIDE F-18

Product Number

1

Dosage Form

-

Strength

10-200mCi/ML

Approval Date

2015-10-23

203968 / 1

Active Ingredient

SODIUM FLUORIDE F-18

Application Number

203968

Product Number

1

Dosage Form

-

Strength

10-200mCi/ML

Approval Date

2015-10-23

Regulatory Status

RX

1982
27 Jan
Discontinued Application: 18272

Drug Name

TECHNESCAN GLUCEPTATE

Product Number

1

Dosage Form

-

Strength

N/A

Approval Date

1982-01-27

18272 / 1

Active Ingredient

TECHNETIUM TC-99M GLUCEPTATE KIT

Application Number

18272

Product Number

1

Dosage Form

-

Strength

N/A

Approval Date

1982-01-27

Regulatory Status

Discontinued

1986
31 Oct
Discontinued Application: 18489

Drug Name

TECHNESCAN HIDA

Product Number

1

Dosage Form

-

Strength

N/A

Approval Date

1986-10-31

18489 / 1

Active Ingredient

TECHNETIUM TC-99M LIDOFENIN KIT

Application Number

18489

Product Number

1

Dosage Form

-

Strength

N/A

Approval Date

1986-10-31

Regulatory Status

Discontinued

-
Unclassified Application: 17881

Drug Name

TECHNETIUM TC 99M ALBUMIN AGGREGATED KIT

Product Number

1

Dosage Form

-

Strength

N/A

Approval Date

-

17881 / 1

Active Ingredient

TECHNETIUM TC-99M ALBUMIN AGGREGATED KIT

Application Number

17881

Product Number

1

Dosage Form

-

Strength

N/A

Approval Date

-

Regulatory Status

Unclassified

2023
30 Jan
RX Application: 216820

Drug Name

TECHNETIUM TC 99M MERTIATIDE KIT

Product Number

1

Dosage Form

-

Strength

N/A

Approval Date

2023-01-30

216820 / 1

Active Ingredient

TECHNETIUM TC-99M MERTIATIDE KIT

Application Number

216820

Product Number

1

Dosage Form

-

Strength

N/A

Approval Date

2023-01-30

Regulatory Status

RX

2009
29 Apr
RX Application: 78806

Drug Name

TECHNETIUM TC 99M SESTAMIBI

Product Number

1

Dosage Form

-

Strength

N/A

Approval Date

2009-04-29

78806 / 1

Active Ingredient

TECHNETIUM TC-99M SESTAMIBI KIT

Application Number

78806

Product Number

1

Dosage Form

-

Strength

N/A

Approval Date

2009-04-29

Regulatory Status

RX

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Drug Status Breakdown
9 total
  • Discontinued
  • RX
  • Unclassified
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

AN-DTPA

Application Number

17714

Product Number

1

Active Ingredient

TECHNETIUM TC-99M PENTETATE KIT

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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