furosemide

Generic: furosemide

Labeler: hikma pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler hikma pharmaceuticals usa inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

furosemide 80 mg/1

Manufacturer
Hikma Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 0054-4301
Product ID 0054-4301_bc62ddda-7639-4090-99f0-7dd4d13518f3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070086
Listing Expiration 2027-12-31
Marketing Start 1991-03-13

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 00544301
Hyphenated Format 0054-4301

Supplemental Identifiers

RxCUI
197730 197731 197732 310429 313988
UPC
0300544301251 0300544299251 0300544297257 0300543298637
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 ANDA070086 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 80 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (0054-4301-25)
  • 500 TABLET in 1 BOTTLE, PLASTIC (0054-4301-29)
source: ndc

Packages (2)

0054-4301-25 100 TABLET in 1 BOTTLE, PLASTIC (0054-4301-25) 0054-4301-29 500 TABLET in 1 BOTTLE, PLASTIC (0054-4301-29)

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": "bc62ddda-7639-4090-99f0-7dd4d13518f3", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0300544301251", "0300544299251", "0300544297257", "0300543298637"], "unii": ["7LXU5N7ZO5"], "rxcui": ["197730", "197731", "197732", "310429", "313988"], "spl_set_id": ["9e493331-dddd-496e-abf8-61747fb67aba"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (0054-4301-25)", "package_ndc": "0054-4301-25", "marketing_start_date": "19910313"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (0054-4301-29)", "package_ndc": "0054-4301-29", "marketing_start_date": "19910313"}], "brand_name": "Furosemide", "product_id": "0054-4301_bc62ddda-7639-4090-99f0-7dd4d13518f3", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "0054-4301", "generic_name": "Furosemide", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "80 mg/1"}], "application_number": "ANDA070086", "marketing_category": "ANDA", "marketing_start_date": "19910313", "listing_expiration_date": "20271231"}