furosemide
Generic: furosemide
Labeler: amneal pharmaceuticals llcDrug Facts
Product Profile
Brand Name
furosemide
Generic Name
furosemide
Labeler
amneal pharmaceuticals llc
Dosage Form
INJECTION
Routes
Active Ingredients
furosemide 20 mg/2mL
Manufacturer
Identifiers & Regulatory
Product NDC
70121-1163
Product ID
70121-1163_0243d363-b856-4a4a-a160-a691ca8c6621
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA207552
Listing Expiration
2026-12-31
Marketing Start
2016-07-25
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
701211163
Hyphenated Format
70121-1163
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
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
ANDA207552 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/2mL
Packaging
- 25 VIAL, GLASS in 1 CARTON (70121-1163-5) / 2 mL in 1 VIAL, GLASS (70121-1163-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "0243d363-b856-4a4a-a160-a691ca8c6621", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0370121107613", "0370121107651", "0370121116356", "0370121116417", "0370121116318", "0370121116455"], "unii": ["7LXU5N7ZO5"], "rxcui": ["1719286", "1719290", "1719291"], "spl_set_id": ["d5b9f12e-d1e9-42de-90f2-c9ba33a86457"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, GLASS in 1 CARTON (70121-1163-5) / 2 mL in 1 VIAL, GLASS (70121-1163-1)", "package_ndc": "70121-1163-5", "marketing_start_date": "20160725"}], "brand_name": "Furosemide", "product_id": "70121-1163_0243d363-b856-4a4a-a160-a691ca8c6621", "dosage_form": "INJECTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "70121-1163", "generic_name": "Furosemide", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "20 mg/2mL"}], "application_number": "ANDA207552", "marketing_category": "ANDA", "marketing_start_date": "20160725", "listing_expiration_date": "20261231"}