Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 018671

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SODIUM IODIDE I 123 (SODIUM IODIDE I-123)
100uCi
Marketing Status: Prescription

Active Ingredient: SODIUM IODIDE I-123
Proprietary Name: SODIUM IODIDE I 123
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 100uCi
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AA
Application Number: N018671
Product Number: 001
Approval Date: May 27, 1982
Applicant Holder Full Name: CARDINAL HEALTH 418 INC
Marketing Status:  Prescription
Patent and Exclusivity Information

SODIUM IODIDE I 123 (SODIUM IODIDE I-123)
200uCi
Marketing Status: Prescription

Active Ingredient: SODIUM IODIDE I-123
Proprietary Name: SODIUM IODIDE I 123
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 200uCi
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AA
Application Number: N018671
Product Number: 002
Approval Date: May 27, 1982
Applicant Holder Full Name: CARDINAL HEALTH 418 INC
Marketing Status:  Prescription
Patent and Exclusivity Information

SODIUM IODIDE I 123 (SODIUM IODIDE I-123)
400uCi
Marketing Status: Discontinued

Active Ingredient: SODIUM IODIDE I-123
Proprietary Name: SODIUM IODIDE I 123
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 400uCi
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N018671
Product Number: 003
Approval Date: May 27, 1982
Applicant Holder Full Name: CARDINAL HEALTH 418 INC
Marketing Status:  Discontinued
Patent and Exclusivity Information