bumetanide

Generic: bumetanide

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name bumetanide
Generic Name bumetanide
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

bumetanide 2 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7350
Product ID 50090-7350_b98f9705-fae8-4aeb-b352-c00942032f1a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209916
Listing Expiration 2026-12-31
Marketing Start 2018-01-30

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 500907350
Hyphenated Format 50090-7350

Supplemental Identifiers

RxCUI
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 ANDA209916 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (50090-7350-0)
source: ndc

Packages (1)

50090-7350-0 90 TABLET in 1 BOTTLE (50090-7350-0)

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": "b98f9705-fae8-4aeb-b352-c00942032f1a", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197419"], "spl_set_id": ["dfa1f77d-8209-48e9-a6c7-d3b4725a97db"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7350-0)", "package_ndc": "50090-7350-0", "marketing_start_date": "20241016"}], "brand_name": "Bumetanide", "product_id": "50090-7350_b98f9705-fae8-4aeb-b352-c00942032f1a", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "50090-7350", "generic_name": "BUMETANIDE", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": "2 mg/1"}], "application_number": "ANDA209916", "marketing_category": "ANDA", "marketing_start_date": "20180130", "listing_expiration_date": "20261231"}