furosemide

Generic: furosemide

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

furosemide 80 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-033
Product ID 72789-033_3c6cb511-4c48-5b4d-e063-6394a90ae712
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 72789033
Hyphenated Format 72789-033

Supplemental Identifiers

RxCUI
197732
UPC
0372789033303
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
  • 80 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (72789-033-01)
  • 30 TABLET in 1 BOTTLE, PLASTIC (72789-033-30)
  • 60 TABLET in 1 BOTTLE, PLASTIC (72789-033-60)
  • 500 TABLET in 1 BOTTLE, PLASTIC (72789-033-82)
source: ndc

Packages (4)

72789-033-01 100 TABLET in 1 BOTTLE, PLASTIC (72789-033-01) 72789-033-30 30 TABLET in 1 BOTTLE, PLASTIC (72789-033-30) 72789-033-60 60 TABLET in 1 BOTTLE, PLASTIC (72789-033-60) 72789-033-82 500 TABLET in 1 BOTTLE, PLASTIC (72789-033-82)

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": "3c6cb511-4c48-5b4d-e063-6394a90ae712", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0372789033303"], "unii": ["7LXU5N7ZO5"], "rxcui": ["197732"], "spl_set_id": ["12137a90-fb35-45d7-8984-0b04793d3e34"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72789-033-01)", "package_ndc": "72789-033-01", "marketing_start_date": "20210309"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-033-30)", "package_ndc": "72789-033-30", "marketing_start_date": "20191209"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (72789-033-60)", "package_ndc": "72789-033-60", "marketing_start_date": "20191209"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (72789-033-82)", "package_ndc": "72789-033-82", "marketing_start_date": "20210309"}], "brand_name": "Furosemide", "product_id": "72789-033_3c6cb511-4c48-5b4d-e063-6394a90ae712", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "72789-033", "generic_name": "furosemide", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "80 mg/1"}], "application_number": "ANDA076796", "marketing_category": "ANDA", "marketing_start_date": "20040326", "listing_expiration_date": "20261231"}