furosemide

Generic: furosemide

Labeler: granulation technology, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler granulation technology, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

furosemide 20 mg/1

Manufacturer
Granulation Technology, Inc.

Identifiers & Regulatory

Product NDC 63561-0164
Product ID 63561-0164_4870846b-dfe5-84bd-e063-6294a90aa56f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018569
Listing Expiration 2027-12-31
Marketing Start 2025-12-18

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 635610164
Hyphenated Format 63561-0164

Supplemental Identifiers

RxCUI
197732 310429 313988
UPC
0363561016492 0363561016423 0363561016652 0363561016515 0363561016591 0363561016522
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 NDA018569 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (63561-0164-1)
  • 1000 TABLET in 1 BOTTLE (63561-0164-2)
  • 90 TABLET in 1 BOTTLE (63561-0164-9)
source: ndc

Packages (3)

63561-0164-1 100 TABLET in 1 BOTTLE (63561-0164-1) 63561-0164-2 1000 TABLET in 1 BOTTLE (63561-0164-2) 63561-0164-9 90 TABLET in 1 BOTTLE (63561-0164-9)

Ingredients (1)

furosemide (20 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": "4870846b-dfe5-84bd-e063-6294a90aa56f", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0363561016492", "0363561016423", "0363561016652", "0363561016515", "0363561016591", "0363561016522"], "unii": ["7LXU5N7ZO5"], "rxcui": ["197732", "310429", "313988"], "spl_set_id": ["462e8917-cbe0-f4f9-e063-6394a90ab4ff"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Granulation Technology, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (63561-0164-1)", "package_ndc": "63561-0164-1", "marketing_start_date": "20260115"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (63561-0164-2)", "package_ndc": "63561-0164-2", "marketing_start_date": "20251218"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (63561-0164-9)", "package_ndc": "63561-0164-9", "marketing_start_date": "20251218"}], "brand_name": "Furosemide", "product_id": "63561-0164_4870846b-dfe5-84bd-e063-6294a90aa56f", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "63561-0164", "generic_name": "FUROSEMIDE", "labeler_name": "Granulation Technology, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "20 mg/1"}], "application_number": "NDA018569", "marketing_category": "NDA", "marketing_start_date": "20251218", "listing_expiration_date": "20271231"}