furosemide

Generic: furosemide

Labeler: camber pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler camber pharmaceuticals, inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

furosemide 10 mg/mL

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-311
Product ID 31722-311_2ce6b13e-910d-7342-e063-6394a90a92ca
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217557
Listing Expiration 2026-12-31
Marketing Start 2024-12-13

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 31722311
Hyphenated Format 31722-311

Supplemental Identifiers

RxCUI
1719286 1719290 1719291
UPC
0331722309318 0331722310314 0331722311106
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 ANDA217557 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
source: ndc
Packaging
  • 25 VIAL, GLASS in 1 BOX (31722-311-31) / 10 mL in 1 VIAL, GLASS (31722-311-10)
source: ndc

Packages (1)

31722-311-31 25 VIAL, GLASS in 1 BOX (31722-311-31) / 10 mL in 1 VIAL, GLASS (31722-311-10)

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": "2ce6b13e-910d-7342-e063-6394a90a92ca", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0331722309318", "0331722310314", "0331722311106"], "unii": ["7LXU5N7ZO5"], "rxcui": ["1719286", "1719290", "1719291"], "spl_set_id": ["f6221cce-e586-4002-bd14-6ec22eb14e2e"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, GLASS in 1 BOX (31722-311-31)  / 10 mL in 1 VIAL, GLASS (31722-311-10)", "package_ndc": "31722-311-31", "marketing_start_date": "20241213"}], "brand_name": "Furosemide", "product_id": "31722-311_2ce6b13e-910d-7342-e063-6394a90a92ca", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "31722-311", "generic_name": "Furosemide", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "10 mg/mL"}], "application_number": "ANDA217557", "marketing_category": "ANDA", "marketing_start_date": "20241213", "listing_expiration_date": "20261231"}