furosemide
Generic: furosemide
Labeler: henry schein, inc.Drug Facts
Product Profile
Brand Name
furosemide
Generic Name
furosemide
Labeler
henry schein, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
furosemide 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0404-9862
Product ID
0404-9862_7dcfd520-5852-49dc-82a6-52a1908e4834
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202747
Listing Expiration
2026-12-31
Marketing Start
2022-01-10
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
04049862
Hyphenated Format
0404-9862
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
ANDA202747 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 1 VIAL, GLASS in 1 BAG (0404-9862-10) / 1 mL in 1 VIAL, GLASS
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "7dcfd520-5852-49dc-82a6-52a1908e4834", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["1719286"], "spl_set_id": ["a9853417-0442-4f53-9543-e0749bc3c80d"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, GLASS in 1 BAG (0404-9862-10) / 1 mL in 1 VIAL, GLASS", "package_ndc": "0404-9862-10", "marketing_start_date": "20220110"}], "brand_name": "FUROSEMIDE", "product_id": "0404-9862_7dcfd520-5852-49dc-82a6-52a1908e4834", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "0404-9862", "generic_name": "furosemide", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FUROSEMIDE", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "10 mg/mL"}], "application_number": "ANDA202747", "marketing_category": "ANDA", "marketing_start_date": "20220110", "listing_expiration_date": "20261231"}