Package 81584-1102-1

Brand: povidone iodine

Generic: povidone-iodine
NDC Package

Package Facts

Identity

Package NDC 81584-1102-1
Digits Only 8158411021
Product NDC 81584-1102
Description

1 TUBE in 1 CARTON (81584-1102-1) / 28.35 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2021-06-30
Brand povidone iodine
Generic povidone-iodine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "7bad4367-4449-46e9-8e5a-61296bc466fd", "openfda": {"nui": ["N0000175486", "M0011640"], "unii": ["85H0HZU99M"], "rxcui": ["312563"], "spl_set_id": ["58e1757c-45ce-455e-bd64-a9e99cd3680f"], "pharm_class_cs": ["Iodine [CS]"], "pharm_class_epc": ["Antiseptic [EPC]"], "manufacturer_name": ["Dr Radows"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (81584-1102-1)  / 28.35 g in 1 TUBE", "package_ndc": "81584-1102-1", "marketing_start_date": "20210630"}], "brand_name": "Povidone Iodine", "product_id": "81584-1102_7bad4367-4449-46e9-8e5a-61296bc466fd", "dosage_form": "OINTMENT", "product_ndc": "81584-1102", "generic_name": "POVIDONE-IODINE", "labeler_name": "Dr Radows", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Povidone Iodine", "active_ingredients": [{"name": "POVIDONE-IODINE", "strength": "100 mg/g"}], "application_number": "M005", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210630", "listing_expiration_date": "20261231"}