furosemide

Generic: furosemide

Labeler: henry schein, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler henry schein, inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

furosemide 20 mg/2mL

Manufacturer
Henry Schein, Inc.

Identifiers & Regulatory

Product NDC 0404-9864
Product ID 0404-9864_9eb5c616-d782-4840-96e6-fbf07bdb916b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212174
Listing Expiration 2026-12-31
Marketing Start 2022-01-10

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 04049864
Hyphenated Format 0404-9864

Supplemental Identifiers

RxCUI
1719290
UNII
7LXU5N7ZO5
NUI
N0000175366 N0000175590

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 ANDA212174 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 20 mg/2mL
source: ndc
Packaging
  • 1 VIAL in 1 BAG (0404-9864-02) / 2 mL in 1 VIAL
source: ndc

Packages (1)

0404-9864-02 1 VIAL in 1 BAG (0404-9864-02) / 2 mL in 1 VIAL

Ingredients (1)

furosemide (20 mg/2mL)

Linked Drug Pages (1)

FUROSEMIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "9eb5c616-d782-4840-96e6-fbf07bdb916b", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["1719290"], "spl_set_id": ["15e4c3a3-7d64-471e-bfdf-6156731e24aa"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BAG (0404-9864-02)  / 2 mL in 1 VIAL", "package_ndc": "0404-9864-02", "marketing_start_date": "20220110"}], "brand_name": "FUROSEMIDE", "product_id": "0404-9864_9eb5c616-d782-4840-96e6-fbf07bdb916b", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "0404-9864", "generic_name": "furosemide", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FUROSEMIDE", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "20 mg/2mL"}], "application_number": "ANDA212174", "marketing_category": "ANDA", "marketing_start_date": "20220110", "listing_expiration_date": "20261231"}