Package 23155-473-42
Brand: furosemide
Generic: furosemidePackage Facts
Identity
Package NDC
23155-473-42
Digits Only
2315547342
Product NDC
23155-473
Description
25 VIAL in 1 CARTON (23155-473-42) / 4 mL in 1 VIAL (23155-473-32)
Marketing
Marketing Status
Brand
furosemide
Generic
furosemide
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "936eaafa-5088-4ebc-85bc-685ffb85c81f", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0323155473315", "0323155473414", "0323155473322", "0323155473339"], "unii": ["7LXU5N7ZO5"], "rxcui": ["1719286", "1719290", "1719291"], "spl_set_id": ["1b9117d5-0dd9-4577-a1fd-bb0aaf7e68ec"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (23155-473-41) / 2 mL in 1 VIAL (23155-473-31)", "package_ndc": "23155-473-41", "marketing_start_date": "20140902"}, {"sample": false, "description": "25 VIAL in 1 CARTON (23155-473-42) / 4 mL in 1 VIAL (23155-473-32)", "package_ndc": "23155-473-42", "marketing_start_date": "20140902"}, {"sample": false, "description": "50 VIAL in 1 CARTON (23155-473-43) / 4 mL in 1 VIAL (23155-473-32)", "package_ndc": "23155-473-43", "marketing_start_date": "20140902"}, {"sample": false, "description": "25 VIAL in 1 CARTON (23155-473-44) / 10 mL in 1 VIAL (23155-473-33)", "package_ndc": "23155-473-44", "marketing_start_date": "20140902"}, {"sample": false, "description": "50 VIAL in 1 CARTON (23155-473-45) / 10 mL in 1 VIAL (23155-473-33)", "package_ndc": "23155-473-45", "marketing_start_date": "20140902"}], "brand_name": "Furosemide", "product_id": "23155-473_936eaafa-5088-4ebc-85bc-685ffb85c81f", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "23155-473", "generic_name": "Furosemide", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "10 mg/mL"}], "application_number": "ANDA203428", "marketing_category": "ANDA", "marketing_start_date": "20140902", "listing_expiration_date": "20261231"}