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Sodium Iodide I-131 - 0019-N450-FC - (sodium iodide, i-131)

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Drug Information of Sodium Iodide I-131

Product NDC: 0019-N450
Proprietary Name: Sodium Iodide I-131
Non Proprietary Name: sodium iodide, i-131
Active Ingredient(s): 5    mCi/mL & nbsp;   sodium iodide, i-131
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Sodium Iodide I-131

Product NDC: 0019-N450
Labeler Name: Mallinckrodt Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA016515
Marketing Category: NDA
Start Marketing Date: 20110822

Package Information of Sodium Iodide I-131

Package NDC: 0019-N450-FC
Package Description: 1 VIAL in 1 CAN (0019-N450-FC) > 15 mL in 1 VIAL

NDC Information of Sodium Iodide I-131

NDC Code 0019-N450-FC
Proprietary Name Sodium Iodide I-131
Package Description 1 VIAL in 1 CAN (0019-N450-FC) > 15 mL in 1 VIAL
Product NDC 0019-N450
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sodium iodide, i-131
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20110822
Marketing Category Name NDA
Labeler Name Mallinckrodt Inc.
Substance Name SODIUM IODIDE I-131
Strength Number 5
Strength Unit mCi/mL
Pharmaceutical Classes Radioactive Therapeutic Agent [EPC],Radiopharmaceutical Activity [MoA]

Complete Information of Sodium Iodide I-131


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