bumetanide

Generic: bumetanide

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name bumetanide
Generic Name bumetanide
Labeler american health packaging
Dosage Form TABLET
Routes
ORAL
Active Ingredients

bumetanide 1 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-384
Product ID 60687-384_21374d66-9881-6023-e063-6394a90a39d2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA018225
Listing Expiration 2026-12-31
Marketing Start 2018-08-02

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 60687384
Hyphenated Format 60687-384

Supplemental Identifiers

RxCUI
197418 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 NDA018225 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-384-01) / 1 TABLET in 1 BLISTER PACK (60687-384-11)
  • 50 BLISTER PACK in 1 CARTON (60687-384-65) / 1 TABLET in 1 BLISTER PACK (60687-384-11)
source: ndc

Packages (2)

60687-384-01 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-384-01) / 1 TABLET in 1 BLISTER PACK (60687-384-11) 60687-384-65 50 BLISTER PACK in 1 CARTON (60687-384-65) / 1 TABLET in 1 BLISTER PACK (60687-384-11)

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": "21374d66-9881-6023-e063-6394a90a39d2", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197418", "197419"], "spl_set_id": ["5e9633e4-151b-4f40-885e-8f364f6f2d18"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-384-01)  / 1 TABLET in 1 BLISTER PACK (60687-384-11)", "package_ndc": "60687-384-01", "marketing_start_date": "20200713"}, {"sample": false, "description": "50 BLISTER PACK in 1 CARTON (60687-384-65)  / 1 TABLET in 1 BLISTER PACK (60687-384-11)", "package_ndc": "60687-384-65", "marketing_start_date": "20230605"}], "brand_name": "Bumetanide", "product_id": "60687-384_21374d66-9881-6023-e063-6394a90a39d2", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "60687-384", "generic_name": "Bumetanide", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": "1 mg/1"}], "application_number": "NDA018225", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20180802", "listing_expiration_date": "20261231"}