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 ID: 48815-1001_c07d2306-68cc-4c33-9b6f-4750c0edf625
• NDC: 48815-1001
• Product Type: Human Prescription Drug
• Proprietary Name: Sodium Iodide I 123
• Generic Name: Sodium Iodide I 123
• Dosage Form: Capsule, Gelatin Coated
• Route of Administration: ORAL
• Marketing Start Date: 2003-01-02
• Marketing Category: NDA / NDA
• Application Number: NDA018671
• Labeler Name: Cardinal Health 418, Inc
• Substance Name: SODIUM IODIDE I-123
• Active Ingredient Strength: 100 uCi/1
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 48815-1001-1

1 VIAL, PLASTIC in 1 CAN (48815-1001-1) > 1 CAPSULE, GELATIN COATED in 1 VIAL, PLASTIC

• Marketing Start Date: 2003-01-02
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 48815-1001-1 [48815100101]

Sodium Iodide I 123 CAPSULE, GELATIN COATED

• Marketing Category: NDA
• Application Number: NDA018671
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2003-01-02

NDC 48815-1001-5 [48815100105]

Sodium Iodide I 123 CAPSULE, GELATIN COATED

• Marketing Category: NDA
• Application Number: NDA018671
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2003-01-02

Drug Details

Active Ingredients

Ingredient	Strength
SODIUM IODIDE I-123	100 uCi/1

OpenFDA Data

• SPL SET ID: 50415c27-1928-4307-b1dc-648f47edf65d
• Manufacturer:
  • Cardinal Health 418, Inc
• UNII:
  • 29UKX3A616

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

NDC	Brand Name	Generic Name
48815-1001	Sodium Iodide I 123	Sodium Iodide I 123
48815-1002	Sodium Iodide I 123	Sodium Iodide I 123
69945-601	SODIUM IODIDE I 123	sodium iodide i 123
69945-602	SODIUM IODIDE I 123	sodium iodide i 123