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
- 70756-618_d4f07f52-c316-401b-b852-a1b29e3570b8
- Product NDC
- 70756-618
- Form
- INJECTION, SOLUTION
- Composition / generic term
- furosemide
- Labeler
- Lifestar Pharma LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20221217
- Source listing expiry
- 20261231
Source-listed ingredients
- FUROSEMIDE — 10 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 5 VIAL in 1 CARTON (70756-618-05) / 2 mL in 1 VIAL (70756-618-82) · 70756-618-05
- 25 VIAL in 1 CARTON (70756-618-25) / 2 mL in 1 VIAL (70756-618-82) · 70756-618-25
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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