furosemide

Generic: furosemide

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

furosemide 80 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 63629-1120
Product ID 63629-1120_620c9a96-bc8b-4966-ab6d-3a77ecb29747
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076796
Listing Expiration 2026-12-31
Marketing Start 2020-07-30

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 636291120
Hyphenated Format 63629-1120

Supplemental Identifiers

RxCUI
197732
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 ANDA076796 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 80 mg/1
source: ndc
Packaging
  • 500 TABLET in 1 BOTTLE, PLASTIC (63629-1120-1)
source: ndc

Packages (1)

63629-1120-1 500 TABLET in 1 BOTTLE, PLASTIC (63629-1120-1)

Ingredients (1)

furosemide (80 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": "620c9a96-bc8b-4966-ab6d-3a77ecb29747", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["197732"], "spl_set_id": ["01a5f094-b473-4e46-9e61-69d5ec6dd766"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (63629-1120-1)", "package_ndc": "63629-1120-1", "marketing_start_date": "20200730"}], "brand_name": "Furosemide", "product_id": "63629-1120_620c9a96-bc8b-4966-ab6d-3a77ecb29747", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "63629-1120", "generic_name": "furosemide", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "80 mg/1"}], "application_number": "ANDA076796", "marketing_category": "ANDA", "marketing_start_date": "20200730", "listing_expiration_date": "20261231"}