Package 72162-2423-2

Brand: potassium iodide

Generic: potassium iodide
NDC Package

Package Facts

Identity

Package NDC 72162-2423-2
Digits Only 7216224232
Product NDC 72162-2423
Description

237 mL in 1 BOTTLE (72162-2423-2)

Marketing

Marketing Status
Marketed Since 2024-11-11
Brand potassium iodide
Generic potassium iodide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1312d1fa-6c50-4d5b-99d0-dcd9c0fe8a13", "openfda": {"unii": ["1C4QK22F9J"], "rxcui": ["312541"], "spl_set_id": ["90cf3abb-c6d4-4004-8ae2-f528260a72f4"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE (72162-2423-2)", "package_ndc": "72162-2423-2", "marketing_start_date": "20241111"}, {"sample": false, "description": "30 mL in 1 BOTTLE, WITH APPLICATOR (72162-2423-3)", "package_ndc": "72162-2423-3", "marketing_start_date": "20241111"}], "brand_name": "POTASSIUM IODIDE", "product_id": "72162-2423_1312d1fa-6c50-4d5b-99d0-dcd9c0fe8a13", "dosage_form": "SOLUTION", "product_ndc": "72162-2423", "generic_name": "POTASSIUM IODIDE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM IODIDE", "active_ingredients": [{"name": "POTASSIUM IODIDE", "strength": "1 g/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20211229", "listing_expiration_date": "20261231"}