furosemide

Generic: furosemide

Labeler: fresenius kabi usa, llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler fresenius kabi usa, llc
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

furosemide 10 mg/mL

Manufacturer
Fresenius Kabi USA, LLC

Identifiers & Regulatory

Product NDC 63323-280
Product ID 63323-280_9804efac-5457-417a-8de7-a688467759c0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018902
Listing Expiration 2026-12-31
Marketing Start 2000-07-12

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 63323280
Hyphenated Format 63323-280

Supplemental Identifiers

RxCUI
1719286 1719290 1719291
UPC
0363323280451 0363323280437 0363323280413
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 NDA018902 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
source: ndc
Packaging
  • 25 VIAL in 1 TRAY (63323-280-16) / 2 mL in 1 VIAL (63323-280-41)
  • 25 VIAL in 1 TRAY (63323-280-26) / 4 mL in 1 VIAL (63323-280-43)
  • 25 VIAL in 1 TRAY (63323-280-36) / 10 mL in 1 VIAL (63323-280-45)
source: ndc

Packages (3)

63323-280-16 25 VIAL in 1 TRAY (63323-280-16) / 2 mL in 1 VIAL (63323-280-41) 63323-280-26 25 VIAL in 1 TRAY (63323-280-26) / 4 mL in 1 VIAL (63323-280-43) 63323-280-36 25 VIAL in 1 TRAY (63323-280-36) / 10 mL in 1 VIAL (63323-280-45)

Ingredients (1)

furosemide (10 mg/mL)

Linked Drug Pages (2)

Furosemide ndc-match (0.9) Furosemide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "9804efac-5457-417a-8de7-a688467759c0", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0363323280451", "0363323280437", "0363323280413"], "unii": ["7LXU5N7ZO5"], "rxcui": ["1719286", "1719290", "1719291"], "spl_set_id": ["3747bbcd-783d-4baa-bb5b-b6827bf390e3"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 TRAY (63323-280-16)  / 2 mL in 1 VIAL (63323-280-41)", "package_ndc": "63323-280-16", "marketing_start_date": "20000712"}, {"sample": false, "description": "25 VIAL in 1 TRAY (63323-280-26)  / 4 mL in 1 VIAL (63323-280-43)", "package_ndc": "63323-280-26", "marketing_start_date": "20000712"}, {"sample": false, "description": "25 VIAL in 1 TRAY (63323-280-36)  / 10 mL in 1 VIAL (63323-280-45)", "package_ndc": "63323-280-36", "marketing_start_date": "20000712"}], "brand_name": "Furosemide", "product_id": "63323-280_9804efac-5457-417a-8de7-a688467759c0", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "63323-280", "generic_name": "FUROSEMIDE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "10 mg/mL"}], "application_number": "NDA018902", "marketing_category": "NDA", "marketing_start_date": "20000712", "listing_expiration_date": "20261231"}