furosemide

Generic: furosemide

Labeler: northwind health company, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler northwind health company, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

furosemide 20 mg/1

Manufacturer
Northwind Health Company, LLC

Identifiers & Regulatory

Product NDC 82868-050
Product ID 82868-050_476ccce7-7a09-d249-e063-6394a90a9af4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216629
Listing Expiration 2027-12-31
Marketing Start 2024-02-29

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 82868050
Hyphenated Format 82868-050

Supplemental Identifiers

RxCUI
310429
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 ANDA216629 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (82868-050-30)
  • 90 TABLET in 1 BOTTLE, PLASTIC (82868-050-90)
source: ndc

Packages (2)

82868-050-30 30 TABLET in 1 BOTTLE, PLASTIC (82868-050-30) 82868-050-90 90 TABLET in 1 BOTTLE, PLASTIC (82868-050-90)

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": "476ccce7-7a09-d249-e063-6394a90a9af4", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["310429"], "spl_set_id": ["13ba97a7-598a-76a4-e063-6294a90a45c5"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (82868-050-30)", "package_ndc": "82868-050-30", "marketing_start_date": "20240229"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (82868-050-90)", "package_ndc": "82868-050-90", "marketing_start_date": "20240229"}], "brand_name": "Furosemide", "product_id": "82868-050_476ccce7-7a09-d249-e063-6394a90a9af4", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "82868-050", "generic_name": "Furosemide", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "20 mg/1"}], "application_number": "ANDA216629", "marketing_category": "ANDA", "marketing_start_date": "20240229", "listing_expiration_date": "20271231"}