NDC 48815-1001

Sodium Iodide I 123

Sodium Iodide I 123

Sodium Iodide I 123 is a Oral Capsule, Gelatin Coated in the Human Prescription Drug category. It is labeled and distributed by Cardinal Health 418, Inc. The primary component is Sodium Iodide I-123.

Product ID48815-1001_c07d2306-68cc-4c33-9b6f-4750c0edf625
NDC48815-1001
Product TypeHuman Prescription Drug
Proprietary NameSodium Iodide I 123
Generic NameSodium Iodide I 123
Dosage FormCapsule, Gelatin Coated
Route of AdministrationORAL
Marketing Start Date2003-01-02
Marketing CategoryNDA / NDA
Application NumberNDA018671
Labeler NameCardinal Health 418, Inc
Substance NameSODIUM IODIDE I-123
Active Ingredient Strength100 uCi/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 48815-1001-1

1 VIAL, PLASTIC in 1 CAN (48815-1001-1) > 1 CAPSULE, GELATIN COATED in 1 VIAL, PLASTIC
Marketing Start Date2003-01-02
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 48815-1001-1 [48815100101]

Sodium Iodide I 123 CAPSULE, GELATIN COATED
Marketing CategoryNDA
Application NumberNDA018671
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2003-01-02

NDC 48815-1001-5 [48815100105]

Sodium Iodide I 123 CAPSULE, GELATIN COATED
Marketing CategoryNDA
Application NumberNDA018671
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2003-01-02

Drug Details

Active Ingredients

IngredientStrength
SODIUM IODIDE I-123100 uCi/1

OpenFDA Data

SPL SET ID:50415c27-1928-4307-b1dc-648f47edf65d
Manufacturer
UNII

NDC Crossover Matching brand name "Sodium Iodide I 123" or generic name "Sodium Iodide I 123"

NDCBrand NameGeneric Name
48815-1001Sodium Iodide I 123Sodium Iodide I 123
48815-1002Sodium Iodide I 123Sodium Iodide I 123
69945-601SODIUM IODIDE I 123sodium iodide i 123
69945-602SODIUM IODIDE I 123sodium iodide i 123

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