furosemide
Generic: furosemide
Labeler: hf acquisition co llc, dba healthfirstDrug Facts
Product Profile
Brand Name
furosemide
Generic Name
furosemide
Labeler
hf acquisition co llc, dba healthfirst
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
furosemide 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
51662-1572
Product ID
51662-1572_0f907fa8-d143-b8c3-e063-6394a90a1a2e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA018902
Listing Expiration
2026-12-31
Marketing Start
2021-06-28
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516621572
Hyphenated Format
51662-1572
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
furosemide (source: ndc)
Generic Name
furosemide (source: ndc)
Application Number
NDA018902 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 2 mL in 1 VIAL (51662-1572-1)
- 25 POUCH in 1 CASE (51662-1572-3) / 1 VIAL in 1 POUCH (51662-1572-2) / 2 mL in 1 VIAL
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "0f907fa8-d143-b8c3-e063-6394a90a1a2e", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0363323280017"], "unii": ["7LXU5N7ZO5"], "rxcui": ["1719290"], "spl_set_id": ["c5db2be1-088f-1110-e053-2a95a90acac8"], "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": "2 mL in 1 VIAL (51662-1572-1)", "package_ndc": "51662-1572-1", "marketing_start_date": "20210628"}, {"sample": false, "description": "25 POUCH in 1 CASE (51662-1572-3) / 1 VIAL in 1 POUCH (51662-1572-2) / 2 mL in 1 VIAL", "package_ndc": "51662-1572-3", "marketing_start_date": "20220612"}], "brand_name": "FUROSEMIDE", "product_id": "51662-1572_0f907fa8-d143-b8c3-e063-6394a90a1a2e", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "51662-1572", "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": "NDA018902", "marketing_category": "NDA", "marketing_start_date": "20210628", "listing_expiration_date": "20261231"}