bumetanide

Generic: bumetanide

Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name bumetanide
Generic Name bumetanide
Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

bumetanide 1 mg/1

Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-901
Product ID 23155-901_ee0c44ac-10ca-4d9b-98f0-1342fc97dd39
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074225
Listing Expiration 2026-12-31
Marketing Start 2024-06-28

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 23155901
Hyphenated Format 23155-901

Supplemental Identifiers

RxCUI
197417 197418 197419
UPC
0323155901016 0323155902013 0323155900019
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
  • 1 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (23155-901-01)
  • 500 TABLET in 1 BOTTLE (23155-901-05)
  • 1000 TABLET in 1 BOTTLE (23155-901-10)
source: ndc

Packages (3)

23155-901-01 100 TABLET in 1 BOTTLE (23155-901-01) 23155-901-05 500 TABLET in 1 BOTTLE (23155-901-05) 23155-901-10 1000 TABLET in 1 BOTTLE (23155-901-10)

Ingredients (1)

bumetanide (1 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": "ee0c44ac-10ca-4d9b-98f0-1342fc97dd39", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0323155901016", "0323155902013", "0323155900019"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197417", "197418", "197419"], "spl_set_id": ["d4688d53-9baf-4cf0-b37f-47779bce7815"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (23155-901-01)", "package_ndc": "23155-901-01", "marketing_start_date": "20240628"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (23155-901-05)", "package_ndc": "23155-901-05", "marketing_start_date": "20240628"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (23155-901-10)", "package_ndc": "23155-901-10", "marketing_start_date": "20240628"}], "brand_name": "bumetanide", "product_id": "23155-901_ee0c44ac-10ca-4d9b-98f0-1342fc97dd39", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "23155-901", "generic_name": "bumetanide", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": "1 mg/1"}], "application_number": "ANDA074225", "marketing_category": "ANDA", "marketing_start_date": "20240628", "listing_expiration_date": "20261231"}