Package 81351-004-02

Brand: saninta 10% povidone-iodine

Generic: povidone-iodine solution
NDC Package

Package Facts

Identity

Package NDC 81351-004-02
Digits Only 8135100402
Product NDC 81351-004
Description

22.5 mL in 1 PACKET (81351-004-02)

Marketing

Marketing Status
Discontinued 2029-09-30
Brand saninta 10% povidone-iodine
Generic povidone-iodine solution
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "47446355-315f-6485-e063-6294a90a0377", "openfda": {"nui": ["N0000175486", "M0011640"], "upc": ["0628634499061"], "unii": ["85H0HZU99M"], "rxcui": ["797730"], "spl_set_id": ["bd344007-895e-30d6-e053-2a95a90a019d"], "pharm_class_cs": ["Iodine [CS]"], "pharm_class_epc": ["Antiseptic [EPC]"], "manufacturer_name": ["LL Pharma"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 APPLICATOR in 1 POUCH (81351-004-01)  / 2.3 mL in 1 APPLICATOR", "package_ndc": "81351-004-01", "marketing_end_date": "20290731", "marketing_start_date": "20210825"}, {"sample": false, "description": "22.5 mL in 1 PACKET (81351-004-02)", "package_ndc": "81351-004-02", "marketing_end_date": "20290930", "marketing_start_date": "20210825"}], "brand_name": "Saninta 10% Povidone-Iodine", "product_id": "81351-004_47446355-315f-6485-e063-6294a90a0377", "dosage_form": "LIQUID", "product_ndc": "81351-004", "generic_name": "Povidone-Iodine Solution", "labeler_name": "LL Pharma", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Saninta 10% Povidone-Iodine", "active_ingredients": [{"name": "POVIDONE-IODINE", "strength": "100 mg/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20290930", "marketing_start_date": "20210825"}