bumetanide

Generic: bumetanide

Labeler: northstar rx, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name bumetanide
Generic Name bumetanide
Labeler northstar rx, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

bumetanide .5 mg/1

Manufacturer
NorthStar Rx, LLC

Identifiers & Regulatory

Product NDC 72603-297
Product ID 72603-297_3aa9066b-354b-4f6b-87b9-2752a3a51f6b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074225
Listing Expiration 2026-12-31
Marketing Start 2025-09-01

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 72603297
Hyphenated Format 72603-297

Supplemental Identifiers

RxCUI
197417 197418 197419
UPC
0372603298017 0372603297010 0372603299014
UNII
0Y2S3XUQ5H
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 bumetanide (source: ndc)
Generic Name bumetanide (source: ndc)
Application Number ANDA074225 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (72603-297-01)
source: ndc

Packages (1)

72603-297-01 100 TABLET in 1 BOTTLE (72603-297-01)

Ingredients (1)

bumetanide (.5 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": "3aa9066b-354b-4f6b-87b9-2752a3a51f6b", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0372603298017", "0372603297010", "0372603299014"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197417", "197418", "197419"], "spl_set_id": ["6b92460e-48ba-44bb-9b61-5e65e5fd82cd"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["NorthStar Rx, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72603-297-01)", "package_ndc": "72603-297-01", "marketing_start_date": "20250901"}], "brand_name": "bumetanide", "product_id": "72603-297_3aa9066b-354b-4f6b-87b9-2752a3a51f6b", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "72603-297", "generic_name": "bumetanide", "labeler_name": "NorthStar Rx, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": ".5 mg/1"}], "application_number": "ANDA074225", "marketing_category": "ANDA", "marketing_start_date": "20250901", "listing_expiration_date": "20261231"}