United States · FDA National Drug Code directory
FUROSCIX
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 71767-100_57ef4d44-0cc5-db23-e063-6294a90a50cc
- Product NDC
- 71767-100
- Form
- INJECTION
- Composition / generic term
- furosemide injection 80 mg/ 10 mL
- Labeler
- scPharmaceuticals Inc., a wholly owned subsidiary of MannKind Corporation
- Marketing category
- NDA
- Marketing start / end (source format)
- 20221114
- Source listing expiry
- 20271231
Source-listed ingredients
- FUROSEMIDE — 8 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 CARTON in 1 KIT (71767-100-01) / 1 CARTRIDGE in 1 CARTON / 10 mL in 1 CARTRIDGE · 71767-100-01
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →