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 .5 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7736
Product ID 50090-7736_1f7a9bc7-10d5-47eb-90b4-a68968996d04
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213942
Listing Expiration 2026-12-31
Marketing Start 2025-01-16

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 500907736
Hyphenated Format 50090-7736

Supplemental Identifiers

RxCUI
197417
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 ANDA213942 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .5 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (50090-7736-0)
source: ndc

Packages (1)

50090-7736-0 90 TABLET in 1 BOTTLE (50090-7736-0)

Ingredients (1)

bumetanide (.5 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": "1f7a9bc7-10d5-47eb-90b4-a68968996d04", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197417"], "spl_set_id": ["14e92f79-2c7b-4ab9-844f-e7bd1964f8b2"], "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 (50090-7736-0)", "package_ndc": "50090-7736-0", "marketing_start_date": "20251028"}], "brand_name": "Bumetanide", "product_id": "50090-7736_1f7a9bc7-10d5-47eb-90b4-a68968996d04", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "50090-7736", "generic_name": "Bumetanide", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": ".5 mg/1"}], "application_number": "ANDA213942", "marketing_category": "ANDA", "marketing_start_date": "20250116", "listing_expiration_date": "20261231"}