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
- 43063-702_4147a2fb-f8a4-1776-e063-6394a90a5185
- Product NDC
- 43063-702
- Form
- TABLET
- Composition / generic term
- Furosemide
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20060201
- Source listing expiry
- 20261231
Source-listed ingredients
- FUROSEMIDE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 21 TABLET in 1 BOTTLE, PLASTIC (43063-702-21) · 43063-702-21
- 30 TABLET in 1 BOTTLE, PLASTIC (43063-702-30) · 43063-702-30
- 60 TABLET in 1 BOTTLE, PLASTIC (43063-702-60) · 43063-702-60
- 1 TABLET in 1 BOTTLE, PLASTIC (43063-702-79) · 43063-702-79
- 90 TABLET in 1 BOTTLE, PLASTIC (43063-702-90) · 43063-702-90
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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