bumetanide

Generic: bumetanide

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name bumetanide
Generic Name bumetanide
Labeler remedyrepack inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

bumetanide 2 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4478
Product ID 70518-4478_3e9b97a1-21dc-4fbb-e063-6394a90afd8c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213942
Listing Expiration 2026-12-31
Marketing Start 2025-09-12

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 705184478
Hyphenated Format 70518-4478

Supplemental Identifiers

RxCUI
197419
UNII
0Y2S3XUQ5H
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 bumetanide (source: ndc)
Generic Name bumetanide (source: ndc)
Application Number ANDA213942 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE, PLASTIC (70518-4478-0)
source: ndc

Packages (1)

70518-4478-0 90 TABLET in 1 BOTTLE, PLASTIC (70518-4478-0)

Ingredients (1)

bumetanide (2 mg/1)

Linked Drug Pages (1)

Bumetanide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3e9b97a1-21dc-4fbb-e063-6394a90afd8c", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197419"], "spl_set_id": ["c5d87c7c-3d03-4a9a-8f07-382371c55169"], "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": "90 TABLET in 1 BOTTLE, PLASTIC (70518-4478-0)", "package_ndc": "70518-4478-0", "marketing_start_date": "20250912"}], "brand_name": "Bumetanide", "product_id": "70518-4478_3e9b97a1-21dc-4fbb-e063-6394a90afd8c", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "70518-4478", "generic_name": "Bumetanide", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": "2 mg/1"}], "application_number": "ANDA213942", "marketing_category": "ANDA", "marketing_start_date": "20250912", "listing_expiration_date": "20261231"}