Package 0065-0411-30

Brand: betadine

Generic: povidone-iodine
NDC Package

Package Facts

Identity

Package NDC 0065-0411-30
Digits Only 0065041130
Product NDC 0065-0411
Description

1 BOTTLE in 1 CARTON (0065-0411-30) / 30 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2000-04-01
Brand betadine
Generic povidone-iodine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "45bf2066-cfd2-48ef-acf9-b590c69b83d8", "openfda": {"nui": ["N0000175486", "M0011640"], "unii": ["85H0HZU99M"], "rxcui": ["312570", "1149663"], "spl_set_id": ["b026de1b-9949-4557-ac49-c7b0038c24cd"], "pharm_class_cs": ["Iodine [CS]"], "pharm_class_epc": ["Antiseptic [EPC]"], "manufacturer_name": ["Alcon Laboratories, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0065-0411-30)  / 30 mL in 1 BOTTLE", "package_ndc": "0065-0411-30", "marketing_start_date": "20000401"}], "brand_name": "Betadine", "product_id": "0065-0411_45bf2066-cfd2-48ef-acf9-b590c69b83d8", "dosage_form": "SOLUTION", "product_ndc": "0065-0411", "generic_name": "povidone-iodine", "labeler_name": "Alcon Laboratories, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Betadine", "active_ingredients": [{"name": "POVIDONE-IODINE", "strength": "5 mg/mL"}], "application_number": "NDA018634", "marketing_category": "NDA", "marketing_start_date": "20000401", "listing_expiration_date": "20261231"}