furoscix

Generic: furosemide injection 80 mg/ 10 ml

Labeler: scpharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name furoscix
Generic Name furosemide injection 80 mg/ 10 ml
Labeler scpharmaceuticals inc.
Dosage Form INJECTION
Routes
SUBCUTANEOUS
Active Ingredients

furosemide 8 mg/mL

Manufacturer
scPharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 71767-100
Product ID 71767-100_46518b53-5ca8-c68b-e063-6394a90a4150
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA209988
Listing Expiration 2026-12-31
Marketing Start 2022-11-14

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 71767100
Hyphenated Format 71767-100

Supplemental Identifiers

RxCUI
2621022 2621028
UPC
0371767100013
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 furoscix (source: ndc)
Generic Name furosemide injection 80 mg/ 10 ml (source: ndc)
Application Number NDA209988 (source: ndc)
Routes
SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 8 mg/mL
source: ndc
Packaging
  • 1 CARTON in 1 KIT (71767-100-01) / 1 CARTRIDGE in 1 CARTON / 10 mL in 1 CARTRIDGE
source: ndc

Packages (1)

Ingredients (1)

furosemide (8 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["SUBCUTANEOUS"], "spl_id": "46518b53-5ca8-c68b-e063-6394a90a4150", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0371767100013"], "unii": ["7LXU5N7ZO5"], "rxcui": ["2621022", "2621028"], "spl_set_id": ["eac958dd-8d43-e44e-e053-2995a90a4d5e"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["scPharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 CARTON in 1 KIT (71767-100-01)  / 1 CARTRIDGE in 1 CARTON / 10 mL in 1 CARTRIDGE", "package_ndc": "71767-100-01", "marketing_start_date": "20221114"}], "brand_name": "FUROSCIX", "product_id": "71767-100_46518b53-5ca8-c68b-e063-6394a90a4150", "dosage_form": "INJECTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "71767-100", "generic_name": "furosemide injection 80 mg/ 10 mL", "labeler_name": "scPharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FUROSCIX", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "8 mg/mL"}], "application_number": "NDA209988", "marketing_category": "NDA", "marketing_start_date": "20221114", "listing_expiration_date": "20261231"}