furosemide

Generic: furosemide

Labeler: qpharma inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler qpharma inc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

furosemide 40 mg/1

Manufacturer
QPharma Inc

Identifiers & Regulatory

Product NDC 42708-123
Product ID 42708-123_459c0c80-5889-208c-e063-6294a90a4d0d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077293
Listing Expiration 2026-12-31
Marketing Start 2006-02-01

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 42708123
Hyphenated Format 42708-123

Supplemental Identifiers

RxCUI
313988
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 ANDA077293 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (42708-123-30)
source: ndc

Packages (1)

42708-123-30 30 TABLET in 1 BOTTLE (42708-123-30)

Ingredients (1)

furosemide (40 mg/1)

Linked Drug Pages (1)

Furosemide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "459c0c80-5889-208c-e063-6294a90a4d0d", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["313988"], "spl_set_id": ["341e29d9-a6f1-4c77-ae44-9b2c423ea6b4"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["QPharma Inc"]}, "finished": true, "packaging": [{"sample": true, "description": "30 TABLET in 1 BOTTLE (42708-123-30)", "package_ndc": "42708-123-30", "marketing_start_date": "20180523"}], "brand_name": "Furosemide", "product_id": "42708-123_459c0c80-5889-208c-e063-6294a90a4d0d", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "42708-123", "generic_name": "Furosemide", "labeler_name": "QPharma Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "40 mg/1"}], "application_number": "ANDA077293", "marketing_category": "ANDA", "marketing_start_date": "20060201", "listing_expiration_date": "20261231"}