furosemide

Generic: furosemide

Labeler: sagent pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler sagent pharmaceuticals
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

furosemide 10 mg/mL

Manufacturer
Sagent Pharmaceuticals

Identifiers & Regulatory

Product NDC 25021-320
Product ID 25021-320_29372fb6-0fa1-4caf-a55f-451091c93390
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214766
Listing Expiration 2026-12-31
Marketing Start 2025-07-15

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 25021320
Hyphenated Format 25021-320

Supplemental Identifiers

RxCUI
1719286 1719290 1719291
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 ANDA214766 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
source: ndc
Packaging
  • 25 VIAL in 1 CARTON (25021-320-02) / 2 mL in 1 VIAL
  • 25 VIAL in 1 CARTON (25021-320-04) / 4 mL in 1 VIAL
  • 25 VIAL in 1 CARTON (25021-320-10) / 10 mL in 1 VIAL
source: ndc

Packages (3)

25021-320-02 25 VIAL in 1 CARTON (25021-320-02) / 2 mL in 1 VIAL 25021-320-04 25 VIAL in 1 CARTON (25021-320-04) / 4 mL in 1 VIAL 25021-320-10 25 VIAL in 1 CARTON (25021-320-10) / 10 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": "29372fb6-0fa1-4caf-a55f-451091c93390", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["1719286", "1719290", "1719291"], "spl_set_id": ["d76bd85a-8e57-477e-9607-c9435f1e26fb"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (25021-320-02)  / 2 mL in 1 VIAL", "package_ndc": "25021-320-02", "marketing_start_date": "20250715"}, {"sample": false, "description": "25 VIAL in 1 CARTON (25021-320-04)  / 4 mL in 1 VIAL", "package_ndc": "25021-320-04", "marketing_start_date": "20250715"}, {"sample": false, "description": "25 VIAL in 1 CARTON (25021-320-10)  / 10 mL in 1 VIAL", "package_ndc": "25021-320-10", "marketing_start_date": "20250715"}], "brand_name": "Furosemide", "product_id": "25021-320_29372fb6-0fa1-4caf-a55f-451091c93390", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "25021-320", "generic_name": "Furosemide", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "10 mg/mL"}], "application_number": "ANDA214766", "marketing_category": "ANDA", "marketing_start_date": "20250715", "listing_expiration_date": "20261231"}