bumetanide

Generic: bumetanide

Labeler: avpak
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name bumetanide
Generic Name bumetanide
Labeler avpak
Dosage Form TABLET
Routes
ORAL
Active Ingredients

bumetanide 2 mg/1

Manufacturer
AvPAK

Identifiers & Regulatory

Product NDC 50268-132
Product ID 50268-132_47e233a3-ffe8-6bf0-e063-6394a90a5b55
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209724
Listing Expiration 2027-12-31
Marketing Start 2019-04-23

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 50268132
Hyphenated Format 50268-132

Supplemental Identifiers

RxCUI
197417 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 ANDA209724 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 50 BLISTER PACK in 1 BOX (50268-132-15) / 1 TABLET in 1 BLISTER PACK (50268-132-11)
source: ndc

Packages (1)

50268-132-15 50 BLISTER PACK in 1 BOX (50268-132-15) / 1 TABLET in 1 BLISTER PACK (50268-132-11)

Ingredients (1)

bumetanide (2 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": "47e233a3-ffe8-6bf0-e063-6394a90a5b55", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197417", "197418", "197419"], "spl_set_id": ["87385a0a-e7e6-8b7f-e053-2991aa0aa21a"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-132-15)  / 1 TABLET in 1 BLISTER PACK (50268-132-11)", "package_ndc": "50268-132-15", "marketing_start_date": "20190423"}], "brand_name": "Bumetanide", "product_id": "50268-132_47e233a3-ffe8-6bf0-e063-6394a90a5b55", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "50268-132", "generic_name": "Bumetanide", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": "2 mg/1"}], "application_number": "ANDA209724", "marketing_category": "ANDA", "marketing_start_date": "20190423", "listing_expiration_date": "20271231"}