Package 75834-280-08

Brand: potassium iodide

Generic: potassium iodide
NDC Package

Package Facts

Identity

Package NDC 75834-280-08
Digits Only 7583428008
Product NDC 75834-280
Description

237 mL in 1 BOTTLE (75834-280-08)

Marketing

Marketing Status
Marketed Since 2021-12-29
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": "62e50e38-f41a-4dc9-96e8-37a7c677bec5", "openfda": {"upc": ["0375834280080", "0375834280301"], "unii": ["1C4QK22F9J"], "rxcui": ["312541"], "spl_set_id": ["b0bf9487-45d0-4fbc-a8dd-90f505355d14"], "manufacturer_name": ["Nivagen Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE (75834-280-08)", "package_ndc": "75834-280-08", "marketing_start_date": "20211229"}, {"sample": false, "description": "30 mL in 1 BOTTLE, WITH APPLICATOR (75834-280-30)", "package_ndc": "75834-280-30", "marketing_start_date": "20211229"}], "brand_name": "POTASSIUM IODIDE", "product_id": "75834-280_62e50e38-f41a-4dc9-96e8-37a7c677bec5", "dosage_form": "SOLUTION", "product_ndc": "75834-280", "generic_name": "POTASSIUM IODIDE", "labeler_name": "Nivagen Pharmaceuticals, Inc.", "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"}