CURIUM US LLC RX
FDA Approved Drugs
CURIUM US LLC 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.
- Total Records 16
- Latest Approval Date Mar 26, 2025
- Data Source FDA
- First Approval Date Jan 01, 1982
Company Snapshot
CURIUM US LLC RX
111 West Port Plaza Suite 800 Saint Louis, MO 63146
U.S.A
www.curiumpharma.com/ View on MapFDA Approved Drug Records ( 16 records )
Drug Name
DETECTNET
Product Number
1
Dosage Form
-
Strength
4mL (1mCi/ML)
Approval Date
2020-09-03
Active Ingredient
COPPER CU-64 DOTATATE
Application Number
213227
Product Number
1
Dosage Form
-
Strength
4mL (1mCi/ML)
Approval Date
2020-09-03
Regulatory Status
RX
Drug Name
GALLIUM CITRATE GA 67
Product Number
1
Dosage Form
-
Strength
2mCi/ML
Approval Date
1982-01-01
Active Ingredient
GALLIUM CITRATE GA-67
Application Number
18058
Product Number
1
Dosage Form
-
Strength
2mCi/ML
Approval Date
1982-01-01
Regulatory Status
RX
Drug Name
IOFLUPANE I-123
Product Number
1
Dosage Form
-
Strength
5mCi/2.5ML (2mCi/ML)
Approval Date
2022-03-30
Active Ingredient
IOFLUPANE I-123
Application Number
213792
Product Number
1
Dosage Form
-
Strength
5mCi/2.5ML (2mCi/ML)
Approval Date
2022-03-30
Regulatory Status
RX
Drug Name
OCTREOSCAN
Product Number
1
Dosage Form
-
Strength
3mCi/ML
Approval Date
1994-06-02
Active Ingredient
INDIUM IN-111 PENTETREOTIDE KIT
Application Number
20314
Product Number
1
Dosage Form
-
Strength
3mCi/ML
Approval Date
1994-06-02
Regulatory Status
RX
Drug Name
SODIUM IODIDE I 123
Product Number
1
Dosage Form
-
Strength
100uCi
Approval Date
1989-02-28
Active Ingredient
SODIUM IODIDE I-123
Application Number
71909
Product Number
1
Dosage Form
-
Strength
100uCi
Approval Date
1989-02-28
Regulatory Status
RX
Drug Name
SODIUM IODIDE I 123
Product Number
1
Dosage Form
-
Strength
200uCi
Approval Date
1989-02-28
Active Ingredient
SODIUM IODIDE I-123
Application Number
71910
Product Number
1
Dosage Form
-
Strength
200uCi
Approval Date
1989-02-28
Regulatory Status
RX
Drug Name
TECHNESCAN HDP
Product Number
1
Dosage Form
-
Strength
N/A
Approval Date
1982-01-01
Active Ingredient
TECHNETIUM TC-99M OXIDRONATE KIT
Application Number
18321
Product Number
1
Dosage Form
-
Strength
N/A
Approval Date
1982-01-01
Regulatory Status
RX
Drug Name
TECHNESCAN MAG3
Product Number
1
Dosage Form
-
Strength
N/A
Approval Date
1990-06-15
Active Ingredient
TECHNETIUM TC-99M MERTIATIDE KIT
Application Number
19882
Product Number
1
Dosage Form
-
Strength
N/A
Approval Date
1990-06-15
Regulatory Status
RX
Drug Name
TECHNESCAN PYP KIT
Product Number
1
Dosage Form
-
Strength
N/A
Approval Date
1982-01-01
Active Ingredient
TECHNETIUM TC-99M PYROPHOSPHATE KIT
Application Number
17538
Product Number
1
Dosage Form
-
Strength
N/A
Approval Date
1982-01-01
Regulatory Status
RX
Drug Name
TECHNETIUM TC 99M SESTAMIBI
Product Number
1
Dosage Form
-
Strength
N/A
Approval Date
2008-09-22
Active Ingredient
TECHNETIUM TC-99M SESTAMIBI KIT
Application Number
78098
Product Number
1
Dosage Form
-
Strength
N/A
Approval Date
2008-09-22
Regulatory Status
RX
Drug Name
TECHNETIUM TC-99M PENTETATE KIT
Product Number
1
Dosage Form
-
Strength
N/A
Approval Date
2025-03-26
Active Ingredient
TECHNETIUM TC-99M PENTETATE KIT
Application Number
215146
Product Number
1
Dosage Form
-
Strength
N/A
Approval Date
2025-03-26
Regulatory Status
RX
Drug Name
THALLOUS CHLORIDE TL 201
Product Number
1
Dosage Form
-
Strength
1mCi/ML
Approval Date
1982-01-01
Active Ingredient
THALLOUS CHLORIDE TL-201
Application Number
18150
Product Number
1
Dosage Form
-
Strength
1mCi/ML
Approval Date
1982-01-01
Regulatory Status
RX
Drug Name
ULTRA-TECHNEKOW V4
Product Number
3
Dosage Form
-
Strength
1-19 CI/GENERATOR
Approval Date
2014-02-18
Active Ingredient
TECHNETIUM TC-99M SODIUM PERTECHNETATE GENERATOR
Application Number
17243
Product Number
3
Dosage Form
-
Strength
1-19 CI/GENERATOR
Approval Date
2014-02-18
Regulatory Status
RX
Drug Name
ULTRATAG
Product Number
1
Dosage Form
-
Strength
N/A
Approval Date
1991-06-10
Active Ingredient
TECHNETIUM TC-99M RED BLOOD CELL KIT
Application Number
19981
Product Number
1
Dosage Form
-
Strength
N/A
Approval Date
1991-06-10
Regulatory Status
RX
Drug Name
XENON XE 133
Product Number
1
Dosage Form
-
Strength
10mCi/VIAL
Approval Date
1982-03-09
Active Ingredient
XENON XE-133
Application Number
18327
Product Number
1
Dosage Form
-
Strength
10mCi/VIAL
Approval Date
1982-03-09
Regulatory Status
RX
Drug Name
XENON XE 133
Product Number
2
Dosage Form
-
Strength
20mCi/VIAL
Approval Date
1982-03-09
Active Ingredient
XENON XE-133
Application Number
18327
Product Number
2
Dosage Form
-
Strength
20mCi/VIAL
Approval Date
1982-03-09
Regulatory Status
RX
Drug Status Breakdown
16 total- RX
Official Source
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Drug Name
DETECTNET
Application Number
213227
Product Number
1
Active Ingredient
COPPER CU-64 DOTATATE
Dosage Form
-
Strength
4mL (1mCi/ML)
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