furosemide

Generic: furosemide

Labeler: hikma pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA 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 20 mg/1

Manufacturer
Hikma Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 0054-8297
Product ID 0054-8297_bc62ddda-7639-4090-99f0-7dd4d13518f3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018823
Listing Expiration 2027-12-31
Marketing Start 1983-11-10

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 00548297
Hyphenated Format 0054-8297

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 NDA018823 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 10 BLISTER PACK in 1 CARTON (0054-8297-25) / 10 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

0054-8297-25 10 BLISTER PACK in 1 CARTON (0054-8297-25) / 10 TABLET in 1 BLISTER PACK

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": "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": "10 BLISTER PACK in 1 CARTON (0054-8297-25)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "0054-8297-25", "marketing_start_date": "19831110"}], "brand_name": "Furosemide", "product_id": "0054-8297_bc62ddda-7639-4090-99f0-7dd4d13518f3", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "0054-8297", "generic_name": "Furosemide", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "20 mg/1"}], "application_number": "NDA018823", "marketing_category": "NDA", "marketing_start_date": "19831110", "listing_expiration_date": "20271231"}