Package 72162-1361-0
Brand: furosemide
Generic: furosemidePackage Facts
Identity
Package NDC
72162-1361-0
Digits Only
7216213610
Product NDC
72162-1361
Description
1000 TABLET in 1 BOTTLE, PLASTIC (72162-1361-0)
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": ["ORAL"], "spl_id": "e959fd06-a804-409d-b545-bed5ba0f12ea", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["313988"], "spl_set_id": ["020bc039-9e99-4895-96f8-0c6a556d3e67"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (72162-1361-0)", "package_ndc": "72162-1361-0", "marketing_start_date": "20231004"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72162-1361-1)", "package_ndc": "72162-1361-1", "marketing_start_date": "20231004"}], "brand_name": "Furosemide", "product_id": "72162-1361_e959fd06-a804-409d-b545-bed5ba0f12ea", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "72162-1361", "generic_name": "furosemide", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "40 mg/1"}], "application_number": "ANDA076796", "marketing_category": "ANDA", "marketing_start_date": "20040326", "listing_expiration_date": "20261231"}