Furosemide

Generic: furosemide

Labeler: REMEDYREPACK INC.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Active

Drug Facts

Product Profile

Brand Name Furosemide
Generic Name furosemide
Labeler REMEDYREPACK INC.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

FUROSEMIDE 20 mg/1

Identifiers & Regulatory

Product NDC 70518-3061
Product ID 70518-3061_3e625d3b-aa68-1274-e063-6294a90acc34
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076796
Listing Expiration 2026-12-31
Marketing Start 2021-03-31

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705183061
Hyphenated Format 70518-3061

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
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (70518-3061-3)
  • 7 TABLET in 1 BOTTLE, PLASTIC (70518-3061-5)
source: ndc

Packages (2)

70518-3061-3 30 TABLET in 1 BOTTLE, PLASTIC (70518-3061-3) 70518-3061-5 7 TABLET in 1 BOTTLE, PLASTIC (70518-3061-5)

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": "3e625d3b-aa68-1274-e063-6294a90acc34", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["310429"], "spl_set_id": ["3d312ab0-589c-427b-84da-18887244bfc9"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (70518-3061-3)", "package_ndc": "70518-3061-3", "marketing_start_date": "20240426"}, {"sample": false, "description": "7 TABLET in 1 BOTTLE, PLASTIC (70518-3061-5)", "package_ndc": "70518-3061-5", "marketing_start_date": "20240426"}], "brand_name": "Furosemide", "product_id": "70518-3061_3e625d3b-aa68-1274-e063-6294a90acc34", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "70518-3061", "generic_name": "furosemide", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "20 mg/1"}], "application_number": "ANDA076796", "marketing_category": "ANDA", "marketing_start_date": "20210331", "listing_expiration_date": "20261231"}