furosemide
Generic: furosemide
Labeler: hikma pharmaceuticals usa inc.Drug Facts
Product Profile
Brand Name
furosemide
Generic Name
furosemide
Labeler
hikma pharmaceuticals usa inc.
Dosage Form
INJECTION
Routes
Active Ingredients
furosemide 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0143-9156
Product ID
0143-9156_febcfbde-87d9-4c2f-819f-dfb4a04082f8
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA018267
Listing Expiration
2026-12-31
Marketing Start
2024-08-19
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
01439156
Hyphenated Format
0143-9156
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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
NDA018267 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 10 VIAL, SINGLE-DOSE in 1 CARTON (0143-9156-10) / 4 mL in 1 VIAL, SINGLE-DOSE (0143-9156-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "febcfbde-87d9-4c2f-819f-dfb4a04082f8", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["1719286", "1719290", "1719291", "2683305", "2683306"], "spl_set_id": ["ddfc41a9-37d4-49c1-bbf3-969a98cd649c"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (0143-9156-10) / 4 mL in 1 VIAL, SINGLE-DOSE (0143-9156-01)", "package_ndc": "0143-9156-10", "marketing_start_date": "20240819"}], "brand_name": "Furosemide", "product_id": "0143-9156_febcfbde-87d9-4c2f-819f-dfb4a04082f8", "dosage_form": "INJECTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "0143-9156", "generic_name": "Furosemide", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "10 mg/mL"}], "application_number": "NDA018267", "marketing_category": "NDA", "marketing_start_date": "20240819", "listing_expiration_date": "20261231"}