furosemide
Generic: furosemide
Labeler: propharma distributionDrug Facts
Product Profile
Brand Name
furosemide
Generic Name
furosemide
Labeler
propharma distribution
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
furosemide 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
84549-474
Product ID
84549-474_43053bf7-904f-dba8-e063-6294a90a7174
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203428
Listing Expiration
2026-12-31
Marketing Start
2023-02-01
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
84549474
Hyphenated Format
84549-474
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
ANDA203428 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 10 mL in 1 VIAL (84549-474-25)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "43053bf7-904f-dba8-e063-6294a90a7174", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["1719286"], "spl_set_id": ["43053bf7-9050-dba8-e063-6294a90a7174"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 VIAL (84549-474-25)", "package_ndc": "84549-474-25", "marketing_start_date": "20251010"}], "brand_name": "Furosemide", "product_id": "84549-474_43053bf7-904f-dba8-e063-6294a90a7174", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "84549-474", "generic_name": "Furosemide", "labeler_name": "ProPharma Distribution", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "10 mg/mL"}], "application_number": "ANDA203428", "marketing_category": "ANDA", "marketing_start_date": "20230201", "listing_expiration_date": "20261231"}