Package 69945-602-20

Brand: sodium iodide i 123

Generic: sodium iodide i 123
NDC Package

Package Facts

Identity

Package NDC 69945-602-20
Digits Only 6994560220
Product NDC 69945-602
Product ID 69945-602_24b19127-9a67-0ddf-e063-6394a90ae0b5
Description

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

Marketing

Marketing Status
Marketed Since 2007-04-11
Brand sodium iodide i 123
Generic sodium iodide i 123
Sample Package No

Linked Drug Pages (1)

SODIUM IODIDE I 123 ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "24b19127-9a67-0ddf-e063-6394a90ae0b5", "openfda": {"unii": ["29UKX3A616"], "spl_set_id": ["493fa2ab-4eb0-4434-9739-3079b2f0e272"], "manufacturer_name": ["Curium US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CAN (69945-602-20)  / 1 CAPSULE, GELATIN COATED in 1 BOTTLE", "package_ndc": "69945-602-20", "marketing_start_date": "20070411"}], "brand_name": "SODIUM IODIDE I 123", "product_id": "69945-602_24b19127-9a67-0ddf-e063-6394a90ae0b5", "dosage_form": "CAPSULE, GELATIN COATED", "product_ndc": "69945-602", "generic_name": "sodium iodide i 123", "labeler_name": "Curium US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SODIUM IODIDE I 123", "active_ingredients": [{"name": "SODIUM IODIDE I-123", "strength": "200 uCi/1"}], "application_number": "ANDA071910", "marketing_category": "ANDA", "marketing_start_date": "20070411", "listing_expiration_date": "20261231"}