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Last Updated: November 22, 2024

Details for New Drug Application (NDA): 018671


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NDA 018671 describes SODIUM IODIDE I 123, which is a drug marketed by Cardinal Health 418, Curium, and Ge Healthcare, and is included in four NDAs. It is available from two suppliers. Additional details are available on the SODIUM IODIDE I 123 profile page.

The generic ingredient in SODIUM IODIDE I 123 is sodium iodide i-123. There are one thousand four hundred and seventy-two drug master file entries for this compound. Two suppliers are listed for this compound. Additional details are available on the sodium iodide i-123 profile page.
Summary for 018671
Tradename:SODIUM IODIDE I 123
Applicant:Cardinal Health 418
Ingredient:sodium iodide i-123
Patents:0
Suppliers and Packaging for NDA: 018671
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
SODIUM IODIDE I 123 sodium iodide i-123 CAPSULE;ORAL 018671 NDA Cardinal Health 418, Inc 48815-1001 48815-1001-1 1 VIAL, PLASTIC in 1 CAN (48815-1001-1) / 1 CAPSULE, GELATIN COATED in 1 VIAL, PLASTIC
SODIUM IODIDE I 123 sodium iodide i-123 CAPSULE;ORAL 018671 NDA Cardinal Health 418, Inc 48815-1001 48815-1001-5 1 VIAL, PLASTIC in 1 CAN (48815-1001-5) / 5 CAPSULE, GELATIN COATED in 1 VIAL, PLASTIC

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:CAPSULE;ORALStrength100uCi
Approval Date:May 27, 1982TE:AARLD:Yes

Profile for product number 002

Active Rx/OTC/Discontinued:RXDosage:CAPSULE;ORALStrength200uCi
Approval Date:May 27, 1982TE:AARLD:Yes

Profile for product number 003

Active Rx/OTC/Discontinued:DISCNDosage:CAPSULE;ORALStrength400uCi
Approval Date:May 27, 1982TE:RLD:No

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