bumetanide
Generic: bumetanide
Labeler: cardinal health 107, llcDrug Facts
Product Profile
Brand Name
bumetanide
Generic Name
bumetanide
Labeler
cardinal health 107, llc
Dosage Form
TABLET
Routes
Active Ingredients
bumetanide 1 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
55154-3572
Product ID
55154-3572_dec479b8-34ca-42af-a455-66e1405e18e7
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209724
Listing Expiration
2027-12-31
Marketing Start
2017-10-18
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
551543572
Hyphenated Format
55154-3572
Supplemental Identifiers
RxCUI
UNII
NUI
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
source: ndc
Resolved Composition
Strengths
- 1 mg/1
Packaging
- 10 BLISTER PACK in 1 BAG (55154-3572-0) / 1 TABLET in 1 BLISTER PACK
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "dec479b8-34ca-42af-a455-66e1405e18e7", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197418"], "spl_set_id": ["9bd4fcd3-3020-41f2-b112-023b5db4487d"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-3572-0) / 1 TABLET in 1 BLISTER PACK", "package_ndc": "55154-3572-0", "marketing_start_date": "20171018"}], "brand_name": "Bumetanide", "product_id": "55154-3572_dec479b8-34ca-42af-a455-66e1405e18e7", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "55154-3572", "generic_name": "Bumetanide", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": "1 mg/1"}], "application_number": "ANDA209724", "marketing_category": "ANDA", "marketing_start_date": "20171018", "listing_expiration_date": "20271231"}