Details for New Drug Application (NDA): 018671
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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: | RX | Dosage: | CAPSULE;ORAL | Strength | 100uCi | ||||
Approval Date: | May 27, 1982 | TE: | AA | RLD: | Yes |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | 200uCi | ||||
Approval Date: | May 27, 1982 | TE: | AA | RLD: | Yes |
Profile for product number 003
Active Rx/OTC/Discontinued: | DISCN | Dosage: | CAPSULE;ORAL | Strength | 400uCi | ||||
Approval Date: | May 27, 1982 | TE: | RLD: | No |
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