bumetanide

Generic: bumetanide

Labeler: sandoz inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

bumetanide 1 mg/1

Manufacturer
Sandoz Inc

Identifiers & Regulatory

Product NDC 0185-0129
Product ID 0185-0129_c6f31ac9-10d1-4d92-882e-836de10e1ce6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074700
Listing Expiration 2026-12-31
Marketing Start 1996-11-21

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 01850129
Hyphenated Format 0185-0129

Supplemental Identifiers

RxCUI
197418 197419 197417
UPC
0301850128013 0301850129010 0301850130016
UNII
0Y2S3XUQ5H
NUI
N0000175366 N0000175590

Packaging Origin

Original Packager
true

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 ANDA074700 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (0185-0129-01)
  • 500 TABLET in 1 BOTTLE (0185-0129-05)
source: ndc

Packages (2)

0185-0129-01 100 TABLET in 1 BOTTLE (0185-0129-01) 0185-0129-05 500 TABLET in 1 BOTTLE (0185-0129-05)

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": "c6f31ac9-10d1-4d92-882e-836de10e1ce6", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0301850128013", "0301850129010", "0301850130016"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197418", "197419", "197417"], "spl_set_id": ["05cb961d-ac33-4bcf-b04e-411e496c43c1"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0185-0129-01)", "package_ndc": "0185-0129-01", "marketing_start_date": "19961121"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (0185-0129-05)", "package_ndc": "0185-0129-05", "marketing_start_date": "19961121"}], "brand_name": "Bumetanide", "product_id": "0185-0129_c6f31ac9-10d1-4d92-882e-836de10e1ce6", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "0185-0129", "generic_name": "Bumetanide", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": "1 mg/1"}], "application_number": "ANDA074700", "marketing_category": "ANDA", "marketing_start_date": "19961121", "listing_expiration_date": "20261231"}