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SODIUM IODIDE I 131 - 0019-9452-15 - (sodium iodide i 131)

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Drug Information of SODIUM IODIDE I 131

Product NDC: 0019-9452
Proprietary Name: SODIUM IODIDE I 131
Non Proprietary Name: sodium iodide i 131
Active Ingredient(s): 1    mCi/mL & nbsp;   sodium iodide i 131
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, GELATIN COATED
Coding System: National Drug Codes(NDC)

Labeler Information of SODIUM IODIDE I 131

Product NDC: 0019-9452
Labeler Name: Mallinckrodt Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA016517
Marketing Category: NDA
Start Marketing Date: 20120125

Package Information of SODIUM IODIDE I 131

Package NDC: 0019-9452-15
Package Description: 1 CAPSULE in 1 CAN (0019-9452-15) > 15 mL in 1 CAPSULE

NDC Information of SODIUM IODIDE I 131

NDC Code 0019-9452-15
Proprietary Name SODIUM IODIDE I 131
Package Description 1 CAPSULE in 1 CAN (0019-9452-15) > 15 mL in 1 CAPSULE
Product NDC 0019-9452
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sodium iodide i 131
Dosage Form Name CAPSULE, GELATIN COATED
Route Name ORAL
Start Marketing Date 20120125
Marketing Category Name NDA
Labeler Name Mallinckrodt Inc.
Substance Name SODIUM IODIDE I-131
Strength Number 1
Strength Unit mCi/mL
Pharmaceutical Classes Radioactive Therapeutic Agent [EPC],Radiopharmaceutical Activity [MoA]

Complete Information of SODIUM IODIDE I 131


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