Package 84449-002-01
Brand: povidone-lodine prep pad
Generic: povidone-lodine prep padPackage Facts
Identity
Package NDC
84449-002-01
Digits Only
8444900201
Product NDC
84449-002
Description
1 g in 1 PATCH (84449-002-01)
Marketing
Marketing Status
Brand
povidone-lodine prep pad
Generic
povidone-lodine prep pad
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "479e3fc6-918d-5eb5-e063-6394a90ae933", "openfda": {"nui": ["N0000175486", "M0011640"], "unii": ["85H0HZU99M"], "spl_set_id": ["201545b8-0697-5601-e063-6394a90a12f4"], "pharm_class_cs": ["Iodine [CS]"], "pharm_class_epc": ["Antiseptic [EPC]"], "manufacturer_name": ["SHENZHEN BENLIJU BIO-TECH CO.,LTD"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 g in 1 PATCH (84449-002-01)", "package_ndc": "84449-002-01", "marketing_start_date": "20240820"}], "brand_name": "Povidone-lodine prep pad", "product_id": "84449-002_479e3fc6-918d-5eb5-e063-6394a90ae933", "dosage_form": "PATCH", "product_ndc": "84449-002", "generic_name": "Povidone-lodine prep pad", "labeler_name": "SHENZHEN BENLIJU BIO-TECH CO.,LTD", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Povidone-lodine prep pad", "active_ingredients": [{"name": "POVIDONE-IODINE", "strength": "10 mg/g"}], "application_number": "M003", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240820", "listing_expiration_date": "20271231"}