Package 67777-141-51
Brand: dynarex povidone iodine prep solution
Generic: povidone iodine prep solutionPackage Facts
Identity
Package NDC
67777-141-51
Digits Only
6777714151
Product NDC
67777-141
Description
24 BOTTLE in 1 CASE (67777-141-51) / 473 mL in 1 BOTTLE (67777-141-50)
Marketing
Marketing Status
Brand
dynarex povidone iodine prep solution
Generic
povidone iodine prep solution
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "275871a0-3173-c7fa-e063-6394a90ac014", "openfda": {"nui": ["N0000175486", "M0011640"], "upc": ["0616784141329"], "unii": ["85H0HZU99M"], "rxcui": ["312564"], "spl_set_id": ["6bb4d55b-2be7-3549-e053-2a91aa0a2bb0"], "pharm_class_cs": ["Iodine [CS]"], "pharm_class_epc": ["Antiseptic [EPC]"], "manufacturer_name": ["Dynarex Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "48 BOTTLE in 1 CASE (67777-141-31) / 118 mL in 1 BOTTLE (67777-141-30)", "package_ndc": "67777-141-31", "marketing_start_date": "20180508"}, {"sample": false, "description": "24 BOTTLE in 1 CASE (67777-141-41) / 237 mL in 1 BOTTLE (67777-141-40)", "package_ndc": "67777-141-41", "marketing_start_date": "20180508"}, {"sample": false, "description": "24 BOTTLE in 1 CASE (67777-141-51) / 473 mL in 1 BOTTLE (67777-141-50)", "package_ndc": "67777-141-51", "marketing_start_date": "20180508"}, {"sample": false, "description": "4 BOTTLE in 1 CASE (67777-141-61) / 3790 mL in 1 BOTTLE (67777-141-60)", "package_ndc": "67777-141-61", "marketing_start_date": "20180508"}], "brand_name": "Dynarex Povidone Iodine Prep Solution", "product_id": "67777-141_275871a0-3173-c7fa-e063-6394a90ac014", "dosage_form": "LIQUID", "product_ndc": "67777-141", "generic_name": "Povidone Iodine Prep Solution", "labeler_name": "Dynarex Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Dynarex Povidone Iodine Prep Solution", "active_ingredients": [{"name": "POVIDONE-IODINE", "strength": "10 mg/mL"}], "application_number": "M003", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180508", "listing_expiration_date": "20261231"}