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 40 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-716
Product ID 43063-716_4147c7b3-f37e-55db-e063-6294a90aa9fd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077293
Listing Expiration 2026-12-31
Marketing Start 2006-02-01

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 43063716
Hyphenated Format 43063-716

Supplemental Identifiers

RxCUI
313988
UPC
0343063716304
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 ANDA077293 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (43063-716-01)
  • 30 TABLET in 1 BOTTLE, PLASTIC (43063-716-30)
  • 60 TABLET in 1 BOTTLE, PLASTIC (43063-716-60)
  • 90 TABLET in 1 BOTTLE, PLASTIC (43063-716-90)
source: ndc

Packages (4)

43063-716-01 100 TABLET in 1 BOTTLE, PLASTIC (43063-716-01) 43063-716-30 30 TABLET in 1 BOTTLE, PLASTIC (43063-716-30) 43063-716-60 60 TABLET in 1 BOTTLE, PLASTIC (43063-716-60) 43063-716-90 90 TABLET in 1 BOTTLE, PLASTIC (43063-716-90)

Ingredients (1)

furosemide (40 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": "4147c7b3-f37e-55db-e063-6294a90aa9fd", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0343063716304"], "unii": ["7LXU5N7ZO5"], "rxcui": ["313988"], "spl_set_id": ["e20257f6-7cfe-43fa-a672-cc1cb312b83a"], "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 (43063-716-01)", "package_ndc": "43063-716-01", "marketing_start_date": "20170516"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-716-30)", "package_ndc": "43063-716-30", "marketing_start_date": "20161012"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (43063-716-60)", "package_ndc": "43063-716-60", "marketing_start_date": "20161016"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (43063-716-90)", "package_ndc": "43063-716-90", "marketing_start_date": "20170106"}], "brand_name": "Furosemide", "product_id": "43063-716_4147c7b3-f37e-55db-e063-6294a90aa9fd", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "43063-716", "generic_name": "Furosemide", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "40 mg/1"}], "application_number": "ANDA077293", "marketing_category": "ANDA", "marketing_start_date": "20060201", "listing_expiration_date": "20261231"}