bumetanide

Generic: bumetanide

Labeler: hf acquisition co llc, dba healthfirst
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name bumetanide
Generic Name bumetanide
Labeler hf acquisition co llc, dba healthfirst
Dosage Form INJECTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

bumetanide .25 mg/mL

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1449
Product ID 51662-1449_2b395f11-a2e3-6a43-e063-6394a90a4efa
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA079196
Listing Expiration 2026-12-31
Marketing Start 2020-01-11

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 516621449
Hyphenated Format 51662-1449

Supplemental Identifiers

RxCUI
1727569
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 ANDA079196 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • .25 mg/mL
source: ndc
Packaging
  • 4 mL in 1 VIAL (51662-1449-1)
source: ndc

Packages (1)

51662-1449-1 4 mL in 1 VIAL (51662-1449-1)

Ingredients (1)

bumetanide (.25 mg/mL)

Linked Drug Pages (1)

BUMETANIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "2b395f11-a2e3-6a43-e063-6394a90a4efa", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["1727569"], "spl_set_id": ["9bd7a71e-0e78-dae7-e053-2995a90ad110"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "4 mL in 1 VIAL (51662-1449-1)", "package_ndc": "51662-1449-1", "marketing_start_date": "20200111"}], "brand_name": "BUMETANIDE", "product_id": "51662-1449_2b395f11-a2e3-6a43-e063-6394a90a4efa", "dosage_form": "INJECTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "51662-1449", "generic_name": "BUMETANIDE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BUMETANIDE", "active_ingredients": [{"name": "BUMETANIDE", "strength": ".25 mg/mL"}], "application_number": "ANDA079196", "marketing_category": "ANDA", "marketing_start_date": "20200111", "listing_expiration_date": "20261231"}