NDC 69945-602

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 Curium Us Llc. The primary component is Sodium Iodide I-123.

• Product ID: 69945-602_5c34102a-8b53-4384-a901-018608d3aba5
• NDC: 69945-602
• 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: 2007-04-11
• Marketing Category: ANDA / ANDA
• Application Number: ANDA071910
• Labeler Name: Curium US LLC
• Substance Name: SODIUM IODIDE I-123
• Active Ingredient Strength: 200 uCi/1
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 69945-602-20

1 BOTTLE in 1 CAN (69945-602-20) > 1 CAPSULE, GELATIN COATED in 1 BOTTLE

• Marketing Start Date: 2007-04-11
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 69945-602-20 [69945060220]

SODIUM IODIDE I 123 CAPSULE, GELATIN COATED

• Marketing Category: ANDA
• Application Number: ANDA071910
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2007-04-11

Drug Details

Active Ingredients

Ingredient	Strength
SODIUM IODIDE I-123	200 uCi/1

OpenFDA Data

• SPL SET ID: 493fa2ab-4eb0-4434-9739-3079b2f0e272
• Manufacturer:
  • Curium US LLC
• 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