furosemide

Generic: furosemide

Labeler: northstar rx llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler northstar rx llc
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

furosemide 10 mg/mL

Manufacturer
NorthStar Rx LLC

Identifiers & Regulatory

Product NDC 72603-251
Product ID 72603-251_ad1cb298-ee74-429e-81e5-82eb2e6bfd77
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203428
Listing Expiration 2026-12-31
Marketing Start 2023-02-01

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 72603251
Hyphenated Format 72603-251

Supplemental Identifiers

RxCUI
1719286 1719290 1719291
UPC
0372603474015 0372603133011 0372603251012 0372603474251
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 ANDA203428 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
source: ndc
Packaging
  • 25 VIAL in 1 CARTON (72603-251-25) / 4 mL in 1 VIAL (72603-251-01)
source: ndc

Packages (1)

72603-251-25 25 VIAL in 1 CARTON (72603-251-25) / 4 mL in 1 VIAL (72603-251-01)

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": ["INTRAVENOUS"], "spl_id": "ad1cb298-ee74-429e-81e5-82eb2e6bfd77", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0372603474015", "0372603133011", "0372603251012", "0372603474251"], "unii": ["7LXU5N7ZO5"], "rxcui": ["1719286", "1719290", "1719291"], "spl_set_id": ["fc3194a3-7e75-4551-8334-4a5cc22d9f8b"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (72603-251-25)  / 4 mL in 1 VIAL (72603-251-01)", "package_ndc": "72603-251-25", "marketing_start_date": "20230201"}, {"sample": false, "description": "25 VIAL in 1 CARTON (72603-251-25)  / 4 mL in 1 VIAL (72603-251-01)", "package_ndc": "72603-251-25", "marketing_start_date": "20250715"}], "brand_name": "Furosemide", "product_id": "72603-251_ad1cb298-ee74-429e-81e5-82eb2e6bfd77", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "72603-251", "generic_name": "Furosemide", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "10 mg/mL"}], "application_number": "ANDA203428", "marketing_category": "ANDA", "marketing_start_date": "20230201", "listing_expiration_date": "20261231"}