furosemide

Generic: furosemide

Labeler: avkare
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

furosemide 20 mg/1

Manufacturer
AvKARE

Identifiers & Regulatory

Product NDC 42291-468
Product ID 42291-468_485d7945-6751-e159-e063-6294a90a27ce
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076796
Listing Expiration 2027-12-31
Marketing Start 2022-01-04

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 42291468
Hyphenated Format 42291-468

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
  • 100 TABLET in 1 BOTTLE (42291-468-01)
  • 1000 TABLET in 1 BOTTLE (42291-468-10)
  • 90 TABLET in 1 BOTTLE (42291-468-90)
source: ndc

Packages (3)

42291-468-01 100 TABLET in 1 BOTTLE (42291-468-01) 42291-468-10 1000 TABLET in 1 BOTTLE (42291-468-10) 42291-468-90 90 TABLET in 1 BOTTLE (42291-468-90)

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": "485d7945-6751-e159-e063-6294a90a27ce", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["197732", "310429", "313988"], "spl_set_id": ["d4c532be-1f3f-60d3-e053-2995a90a98be"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42291-468-01)", "package_ndc": "42291-468-01", "marketing_start_date": "20220104"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (42291-468-10)", "package_ndc": "42291-468-10", "marketing_start_date": "20220104"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (42291-468-90)", "package_ndc": "42291-468-90", "marketing_start_date": "20220104"}], "brand_name": "Furosemide", "product_id": "42291-468_485d7945-6751-e159-e063-6294a90a27ce", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "42291-468", "generic_name": "furosemide", "labeler_name": "AvKARE", "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": "20220104", "listing_expiration_date": "20271231"}