furosemide
Generic: furosemide
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
furosemide
Generic Name
furosemide
Labeler
a-s medication solutions
Dosage Form
TABLET
Routes
Active Ingredients
furosemide 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-5429
Product ID
50090-5429_3fa7e5ea-da92-4b30-bd78-d92f4d2498de
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077293
Listing Expiration
2026-12-31
Marketing Start
2006-02-01
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500905429
Hyphenated Format
50090-5429
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
furosemide (source: ndc)
Generic Name
furosemide (source: ndc)
Application Number
ANDA077293 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (50090-5429-0)
- 100 TABLET in 1 BOTTLE (50090-5429-1)
- 200 TABLET in 1 BOTTLE (50090-5429-7)
- 90 TABLET in 1 BOTTLE (50090-5429-8)
Packages (4)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3fa7e5ea-da92-4b30-bd78-d92f4d2498de", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["310429"], "spl_set_id": ["52f0c9d5-396f-4033-abe8-145eec3e6983"], "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": "30 TABLET in 1 BOTTLE (50090-5429-0)", "package_ndc": "50090-5429-0", "marketing_start_date": "20210111"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-5429-1)", "package_ndc": "50090-5429-1", "marketing_start_date": "20210111"}, {"sample": false, "description": "200 TABLET in 1 BOTTLE (50090-5429-7)", "package_ndc": "50090-5429-7", "marketing_start_date": "20230117"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-5429-8)", "package_ndc": "50090-5429-8", "marketing_start_date": "20210111"}], "brand_name": "Furosemide", "product_id": "50090-5429_3fa7e5ea-da92-4b30-bd78-d92f4d2498de", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "50090-5429", "generic_name": "Furosemide", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "20 mg/1"}], "application_number": "ANDA077293", "marketing_category": "ANDA", "marketing_start_date": "20060201", "listing_expiration_date": "20261231"}