furosemide

Generic: furosemide

Labeler: ncs healthcare of ky, llc dba vangard labs
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler ncs healthcare of ky, llc dba vangard labs
Dosage Form TABLET
Routes
ORAL
Active Ingredients

furosemide 20 mg/1

Manufacturer
NCS HealthCare of KY, LLC dba Vangard Labs

Identifiers & Regulatory

Product NDC 0615-8368
Product ID 0615-8368_fb99ad62-fc5e-4eab-9f63-20246541729c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076796
Listing Expiration 2026-12-31
Marketing Start 2004-03-26

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 06158368
Hyphenated Format 0615-8368

Supplemental Identifiers

RxCUI
197732 310429 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 ANDA076796 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 15 TABLET in 1 BLISTER PACK (0615-8368-05)
  • 7 TABLET in 1 BLISTER PACK (0615-8368-07)
  • 10 TABLET in 1 BLISTER PACK (0615-8368-10)
  • 14 TABLET in 1 BLISTER PACK (0615-8368-14)
  • 28 TABLET in 1 BLISTER PACK (0615-8368-28)
  • 6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-8368-30) / 5 TABLET in 1 BLISTER PACK
  • 30 TABLET in 1 BLISTER PACK (0615-8368-39)
source: ndc

Packages (7)

0615-8368-05 15 TABLET in 1 BLISTER PACK (0615-8368-05) 0615-8368-07 7 TABLET in 1 BLISTER PACK (0615-8368-07) 0615-8368-10 10 TABLET in 1 BLISTER PACK (0615-8368-10) 0615-8368-14 14 TABLET in 1 BLISTER PACK (0615-8368-14) 0615-8368-28 28 TABLET in 1 BLISTER PACK (0615-8368-28) 0615-8368-30 6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-8368-30) / 5 TABLET in 1 BLISTER PACK 0615-8368-39 30 TABLET in 1 BLISTER PACK (0615-8368-39)

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": "fb99ad62-fc5e-4eab-9f63-20246541729c", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["197732", "310429", "313988"], "spl_set_id": ["114f4f4f-536a-4658-8fd0-2dd8c029b19a"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET in 1 BLISTER PACK (0615-8368-05)", "package_ndc": "0615-8368-05", "marketing_start_date": "20201208"}, {"sample": false, "description": "7 TABLET in 1 BLISTER PACK (0615-8368-07)", "package_ndc": "0615-8368-07", "marketing_start_date": "20220621"}, {"sample": false, "description": "10 TABLET in 1 BLISTER PACK (0615-8368-10)", "package_ndc": "0615-8368-10", "marketing_start_date": "20221118"}, {"sample": false, "description": "14 TABLET in 1 BLISTER PACK (0615-8368-14)", "package_ndc": "0615-8368-14", "marketing_start_date": "20220621"}, {"sample": false, "description": "28 TABLET in 1 BLISTER PACK (0615-8368-28)", "package_ndc": "0615-8368-28", "marketing_start_date": "20240415"}, {"sample": false, "description": "6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-8368-30)  / 5 TABLET in 1 BLISTER PACK", "package_ndc": "0615-8368-30", "marketing_start_date": "20201214"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (0615-8368-39)", "package_ndc": "0615-8368-39", "marketing_start_date": "20201208"}], "brand_name": "Furosemide", "product_id": "0615-8368_fb99ad62-fc5e-4eab-9f63-20246541729c", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "0615-8368", "generic_name": "furosemide", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "20 mg/1"}], "application_number": "ANDA076796", "marketing_category": "ANDA", "marketing_start_date": "20040326", "listing_expiration_date": "20261231"}