Package 68071-4445-6

Brand: furosemide

Generic: furosemide
NDC Package

Package Facts

Identity

Package NDC 68071-4445-6
Digits Only 6807144456
Product NDC 68071-4445
Description

60 TABLET in 1 BOTTLE (68071-4445-6)

Marketing

Marketing Status
Marketed Since 2018-05-21
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": "1a8ce174-9cb5-77f8-e063-6394a90ae5b2", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0368071444599"], "unii": ["7LXU5N7ZO5"], "rxcui": ["313988"], "spl_set_id": ["6cbf3834-0433-4dc0-e053-2a91aa0a8f8a"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (68071-4445-1)", "package_ndc": "68071-4445-1", "marketing_start_date": "20180521"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (68071-4445-2)", "package_ndc": "68071-4445-2", "marketing_start_date": "20180521"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-4445-3)", "package_ndc": "68071-4445-3", "marketing_start_date": "20180521"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (68071-4445-4)", "package_ndc": "68071-4445-4", "marketing_start_date": "20180521"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68071-4445-6)", "package_ndc": "68071-4445-6", "marketing_start_date": "20180521"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (68071-4445-8)", "package_ndc": "68071-4445-8", "marketing_start_date": "20180521"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-4445-9)", "package_ndc": "68071-4445-9", "marketing_start_date": "20180521"}], "brand_name": "Furosemide", "product_id": "68071-4445_1a8ce174-9cb5-77f8-e063-6394a90ae5b2", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "68071-4445", "generic_name": "furosemide", "labeler_name": "NuCare Pharmaceuticals,Inc.", "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"}