furosemide

Generic: furosemide

Labeler: rising pharma holdings, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler rising pharma holdings, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

furosemide 20 mg/1

Manufacturer
Rising Pharma Holdings, Inc.

Identifiers & Regulatory

Product NDC 64980-562
Product ID 64980-562_458b3c62-666c-43f2-8feb-ee8e6cbe8931
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216629
Listing Expiration 2026-12-31
Marketing Start 2022-11-05

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 64980562
Hyphenated Format 64980-562

Supplemental Identifiers

RxCUI
197732 310429 313988
UPC
0364980564014
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 ANDA216629 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (64980-562-01)
  • 1000 TABLET in 1 BOTTLE (64980-562-10)
source: ndc

Packages (2)

64980-562-01 100 TABLET in 1 BOTTLE (64980-562-01) 64980-562-10 1000 TABLET in 1 BOTTLE (64980-562-10)

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": "458b3c62-666c-43f2-8feb-ee8e6cbe8931", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0364980564014"], "unii": ["7LXU5N7ZO5"], "rxcui": ["197732", "310429", "313988"], "spl_set_id": ["6101b9b4-f3ef-438e-a857-b4ea55ffc679"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (64980-562-01)", "package_ndc": "64980-562-01", "marketing_start_date": "20221105"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (64980-562-10)", "package_ndc": "64980-562-10", "marketing_start_date": "20221105"}], "brand_name": "Furosemide", "product_id": "64980-562_458b3c62-666c-43f2-8feb-ee8e6cbe8931", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "64980-562", "generic_name": "Furosemide", "labeler_name": "Rising Pharma Holdings, Inc.", "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": "20221105", "listing_expiration_date": "20261231"}