furosemide

Generic: furosemide

Labeler: amneal pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler amneal pharmaceuticals llc
Dosage Form INJECTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

furosemide 20 mg/2mL

Manufacturer
Amneal Pharmaceuticals LLC

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)
loop diuretic [epc]
Physiologic Effect
increased diuresis at loop of henle [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 701211163
Hyphenated Format 70121-1163

Supplemental Identifiers

RxCUI
1719286 1719290 1719291
UPC
0370121107613 0370121107651 0370121116356 0370121116417 0370121116318 0370121116455
UNII
7LXU5N7ZO5
NUI
N0000175366 N0000175590

Packaging Origin

Original Packager
true

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
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 20 mg/2mL
source: ndc
Packaging
  • 25 VIAL, GLASS in 1 CARTON (70121-1163-5) / 2 mL in 1 VIAL, GLASS (70121-1163-1)
source: ndc

Packages (1)

Ingredients (1)

furosemide (20 mg/2mL)

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"}