CURIUM US LLC Discontinued
FDA Approved Drugs

CURIUM US LLC Discontinued

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
  • Total Records 9
  • Latest Approval Date Nov 09, 2006
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
25
View
Discontinued
9
View
RX
16
View
Company Overview

Company

CURIUM US LLC Discontinued

Country

U.S.A

Website

Visit Website

Email

Social Profiles

Company Snapshot

CURIUM US LLC Discontinued

111 West Port Plaza Suite 800 Saint Louis, MO 63146

U.S.A

www.curiumpharma.com/ View on Map
FDA Approved Drug Records ( 9 records )
1994
27 Sep
Discontinued Application: 19841

Drug Name

INDIUM IN 111 CHLORIDE

Product Number

1

Dosage Form

-

Strength

5mCi/0.5ML

Approval Date

1994-09-27

19841 / 1

Active Ingredient

INDIUM IN-111 CHLORIDE

Application Number

19841

Product Number

1

Dosage Form

-

Strength

5mCi/0.5ML

Approval Date

1994-09-27

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17084

Drug Name

PHOSPHOCOL P32

Product Number

1

Dosage Form

-

Strength

5mCi/ML

Approval Date

1982-01-01

17084 / 1

Active Ingredient

CHROMIC PHOSPHATE P-32

Application Number

17084

Product Number

1

Dosage Form

-

Strength

5mCi/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 16708

Drug Name

SODIUM CHROMATE CR 51

Product Number

1

Dosage Form

-

Strength

100uCi/ML

Approval Date

1982-01-01

16708 / 1

Active Ingredient

SODIUM CHROMATE CR-51

Application Number

16708

Product Number

1

Dosage Form

-

Strength

100uCi/ML

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 16515

Drug Name

SODIUM IODIDE I 131

Product Number

1

Dosage Form

-

Strength

3.5-150mCi/VIAL

Approval Date

1982-01-01

16515 / 1

Active Ingredient

SODIUM IODIDE I-131

Application Number

16515

Product Number

1

Dosage Form

-

Strength

3.5-150mCi/VIAL

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 16515

Drug Name

SODIUM IODIDE I 131

Product Number

2

Dosage Form

-

Strength

0.8-100mCi

Approval Date

1982-01-01

16515 / 2

Active Ingredient

SODIUM IODIDE I-131

Application Number

16515

Product Number

2

Dosage Form

-

Strength

0.8-100mCi

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 16517

Drug Name

SODIUM IODIDE I 131

Product Number

1

Dosage Form

-

Strength

0.8-100mCi

Approval Date

1982-01-01

16517 / 1

Active Ingredient

SODIUM IODIDE I-131

Application Number

16517

Product Number

1

Dosage Form

-

Strength

0.8-100mCi

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 16517

Drug Name

SODIUM IODIDE I 131

Product Number

2

Dosage Form

-

Strength

15-100uCi

Approval Date

1982-01-01

16517 / 2

Active Ingredient

SODIUM IODIDE I-131

Application Number

16517

Product Number

2

Dosage Form

-

Strength

15-100uCi

Approval Date

1982-01-01

Regulatory Status

Discontinued

2006
09 Nov
Discontinued Application: 77698

Drug Name

THALLOUS CHLORIDE TL 201

Product Number

1

Dosage Form

-

Strength

2mCi/ML

Approval Date

2006-11-09

77698 / 1

Active Ingredient

THALLOUS CHLORIDE TL-201

Application Number

77698

Product Number

1

Dosage Form

-

Strength

2mCi/ML

Approval Date

2006-11-09

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 17243

Drug Name

ULTRA-TECHNEKOW V4

Product Number

2

Dosage Form

-

Strength

0.25-3 CI/GENERATOR

Approval Date

1982-01-01

17243 / 2

Active Ingredient

TECHNETIUM TC-99M SODIUM PERTECHNETATE GENERATOR

Application Number

17243

Product Number

2

Dosage Form

-

Strength

0.25-3 CI/GENERATOR

Approval Date

1982-01-01

Regulatory Status

Discontinued

Related Databases
  • FDA Inspections
    2 View
  • EDQM CEP
    0 View
  • KDMF
    0 View
  • Japan DMF
    0 View
  • Eudra GMP
    0 View
  • NDC Database
    4 View
  • FDA Approved Drugs Database
    25 View
  • Drug Prices in Switzerland
    0 View
Drug Status Breakdown
9 total
  • Discontinued
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

INDIUM IN 111 CHLORIDE

Application Number

19841

Product Number

1

Active Ingredient

INDIUM IN-111 CHLORIDE

Dosage Form

-

Strength

5mCi/0.5ML

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