bumetanide

Generic: bumetanide

Labeler: amneal pharmaceuticals ny llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name bumetanide
Generic Name bumetanide
Labeler amneal pharmaceuticals ny llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

bumetanide 1 mg/1

Manufacturer
Amneal Pharmaceuticals NY LLC

Identifiers & Regulatory

Product NDC 69238-1490
Product ID 69238-1490_d1961e90-3fcc-4b72-b207-6c9de6d66557
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209724
Listing Expiration 2026-12-31
Marketing Start 2017-10-18

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 692381490
Hyphenated Format 69238-1490

Supplemental Identifiers

RxCUI
197417 197418 197419
UPC
0369238149111 0369238149012 0369238148916
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 ANDA209724 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (69238-1490-1)
  • 500 TABLET in 1 BOTTLE (69238-1490-5)
source: ndc

Packages (2)

69238-1490-1 100 TABLET in 1 BOTTLE (69238-1490-1) 69238-1490-5 500 TABLET in 1 BOTTLE (69238-1490-5)

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": "d1961e90-3fcc-4b72-b207-6c9de6d66557", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0369238149111", "0369238149012", "0369238148916"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197417", "197418", "197419"], "spl_set_id": ["9188ab17-8539-48a5-905f-ad35ab5a0b93"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69238-1490-1)", "package_ndc": "69238-1490-1", "marketing_start_date": "20171018"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (69238-1490-5)", "package_ndc": "69238-1490-5", "marketing_start_date": "20171018"}], "brand_name": "Bumetanide", "product_id": "69238-1490_d1961e90-3fcc-4b72-b207-6c9de6d66557", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "69238-1490", "generic_name": "Bumetanide", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": "1 mg/1"}], "application_number": "ANDA209724", "marketing_category": "ANDA", "marketing_start_date": "20171018", "listing_expiration_date": "20261231"}