United States · FDA National Drug Code directory
Furosemide
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
- 0409-6102_981d5143-60cd-4987-9b47-dec24c10de42
- Product NDC
- 0409-6102
- Form
- INJECTION, SOLUTION
- Composition / generic term
- FUROSEMIDE
- Labeler
- Hospira, Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20050228
- Source listing expiry
- 20271231
Source-listed ingredients
- FUROSEMIDE — 10 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-6102-02) / 2 mL in 1 VIAL, SINGLE-DOSE (0409-6102-19) · 0409-6102-02
- 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-6102-04) / 4 mL in 1 VIAL, SINGLE-DOSE (0409-6102-18) · 0409-6102-04
- 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-6102-10) / 10 mL in 1 VIAL, SINGLE-DOSE (0409-6102-20) · 0409-6102-10
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 →