furosemide

Generic: furosemide

Labeler: baxter healthcare corporation
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler baxter healthcare corporation
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

furosemide 10 mg/mL

Manufacturer
Baxter Healthcare Corporation

Identifiers & Regulatory

Product NDC 36000-283
Product ID 36000-283_b4c1ae97-0f6c-4ae1-858a-4e0ab8f1ce53
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202747
Listing Expiration 2026-12-31
Marketing Start 2014-02-06

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 36000283
Hyphenated Format 36000-283

Supplemental Identifiers

RxCUI
1719286 1719290 1719291
UPC
0336000063012 0336000065016 0336000283250 0336000282253 0336000064019 0336000284257
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 ANDA202747 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
source: ndc
Packaging
  • 25 VIAL, SINGLE-DOSE in 1 BOX (36000-283-25) / 4 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (1)

36000-283-25 25 VIAL, SINGLE-DOSE in 1 BOX (36000-283-25) / 4 mL in 1 VIAL, SINGLE-DOSE

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": "b4c1ae97-0f6c-4ae1-858a-4e0ab8f1ce53", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0336000063012", "0336000065016", "0336000283250", "0336000282253", "0336000064019", "0336000284257"], "unii": ["7LXU5N7ZO5"], "rxcui": ["1719286", "1719290", "1719291"], "spl_set_id": ["c71371a7-75c5-45b8-b762-8d782d4c71bc"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 BOX (36000-283-25)  / 4 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "36000-283-25", "marketing_start_date": "20140206"}], "brand_name": "FUROSEMIDE", "product_id": "36000-283_b4c1ae97-0f6c-4ae1-858a-4e0ab8f1ce53", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "36000-283", "generic_name": "furosemide", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FUROSEMIDE", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "10 mg/mL"}], "application_number": "ANDA202747", "marketing_category": "ANDA", "marketing_start_date": "20140206", "listing_expiration_date": "20261231"}