furosemide

Generic: furosemide

Labeler: hikma pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler hikma pharmaceuticals usa inc.
Dosage Form INJECTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

furosemide 10 mg/mL

Manufacturer
Hikma Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 0143-9158
Product ID 0143-9158_febcfbde-87d9-4c2f-819f-dfb4a04082f8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018267
Listing Expiration 2026-12-31
Marketing Start 2024-05-31

Pharmacologic Class

Established (EPC)
loop diuretic [epc]
Physiologic Effect
increased diuresis at loop of henle [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01439158
Hyphenated Format 0143-9158

Supplemental Identifiers

RxCUI
1719286 1719290 1719291 2683305 2683306
UNII
7LXU5N7ZO5
NUI
N0000175366 N0000175590

Packaging Origin

Original Packager
true

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
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (0143-9158-01) / 50 mL in 1 VIAL
source: ndc

Packages (1)

0143-9158-01 1 VIAL in 1 CARTON (0143-9158-01) / 50 mL in 1 VIAL

Ingredients (1)

furosemide (10 mg/mL)

Linked Drug Pages (1)

Furosemide ndc-match (0.9)

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": "1 VIAL in 1 CARTON (0143-9158-01)  / 50 mL in 1 VIAL", "package_ndc": "0143-9158-01", "marketing_start_date": "20240531"}], "brand_name": "Furosemide", "product_id": "0143-9158_febcfbde-87d9-4c2f-819f-dfb4a04082f8", "dosage_form": "INJECTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "0143-9158", "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": "20240531", "listing_expiration_date": "20261231"}