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Sodium Iodide I 123Drug - Sodium Iodide I 123 The trade name of the product as shown on the labeling.
Dosage -
CAPSULE; ORAL
Active Ingredient(s) -
Sodium Iodide, I-123
Strength -
100uCi
Applicant -
GE HEALTHCARE
New Drug Application (NDA) Number -
017630
Product Number -
001
Therapeutic Equivalence (TE) Code -
AA
Approval Date -
Approved Prior to Jan 1, 1982
Reference Listed Drug (RLD) -
No
Type -
RX
Applicant Full Name -
Ge Healthcare
Sodium Iodide I 123
Ferrlecit 62.5mg/5ml Injectable; Injection
Fluorine F-18 2mci/ml **federal Register Determination That Product Was Not Discontinued Or Withdrawn For Safety Or Efficacy Reasons** Injectable; Intravenous Colgate Total 0.24%;0.3% Paste; Dental Sodium Iodide I 123 100uci Capsule; Oral Sodium Chloride 0.9% In Plastic Container 900mg/100ml Solution; Irrigation Sodium Chloride 0.9% In Plastic Container 900mg/100ml Solution; Irrigation Sodium Chloride In Plastic Container 900mg/100ml Solution; Irrigation Chromitope Sodium 200uci/ml Injectable; Injection Chromitope Sodium 2mci/vial Injectable; Injection Sodium Chromate Cr 51 100uci/ml Injectable; Injection NewDrugInformation |