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
- 23155-473_c14acada-333e-43bb-b1cf-81d569e3e918
- Product NDC
- 23155-473
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Furosemide
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140902
- Source listing expiry
- 20271231
Source-listed ingredients
- FUROSEMIDE — 10 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 25 VIAL in 1 CARTON (23155-473-41) / 2 mL in 1 VIAL (23155-473-31) · 23155-473-41
- 25 VIAL in 1 CARTON (23155-473-42) / 4 mL in 1 VIAL (23155-473-32) · 23155-473-42
- 50 VIAL in 1 CARTON (23155-473-43) / 4 mL in 1 VIAL (23155-473-32) · 23155-473-43
- 25 VIAL in 1 CARTON (23155-473-44) / 10 mL in 1 VIAL (23155-473-33) · 23155-473-44
- 50 VIAL in 1 CARTON (23155-473-45) / 10 mL in 1 VIAL (23155-473-33) · 23155-473-45
Source and coverage
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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.
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