Package 51662-1226-3

Brand: furosemide

Generic: furosemide
NDC Package

Package Facts

Identity

Package NDC 51662-1226-3
Digits Only 5166212263
Product NDC 51662-1226
Description

25 POUCH in 1 CASE (51662-1226-3) / 1 VIAL, SINGLE-USE in 1 POUCH (51662-1226-2) / 10 mL in 1 VIAL, SINGLE-USE

Marketing

Marketing Status
Marketed Since 2022-04-22
Brand furosemide
Generic furosemide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "0f8e7f56-23e5-8931-e063-6294a90af687", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["1719286"], "spl_set_id": ["75d5611a-f9e0-1841-e053-2991aa0af415"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 VIAL, SINGLE-USE (51662-1226-1)", "package_ndc": "51662-1226-1", "marketing_start_date": "20180914"}, {"sample": false, "description": "25 POUCH in 1 CASE (51662-1226-3)  / 1 VIAL, SINGLE-USE in 1 POUCH (51662-1226-2)  / 10 mL in 1 VIAL, SINGLE-USE", "package_ndc": "51662-1226-3", "marketing_start_date": "20220422"}], "brand_name": "FUROSEMIDE", "product_id": "51662-1226_0f8e7f56-23e5-8931-e063-6294a90af687", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "51662-1226", "generic_name": "FUROSEMIDE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FUROSEMIDE", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "10 mg/mL"}], "application_number": "NDA018667", "marketing_category": "NDA", "marketing_start_date": "20180914", "listing_expiration_date": "20261231"}