United States · FDA National Drug Code directory
Nitrofurantoin
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
- 43386-450_361dd255-19ba-453f-9b68-ade3185ff390
- Product NDC
- 43386-450
- Form
- SUSPENSION
- Composition / generic term
- Nitrofurantoin
- Labeler
- Lupin Pharmaceuticals,Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150521
- Source listing expiry
- 20261231
Source-listed ingredients
- NITROFURANTOIN — 25 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (43386-450-11) / 230 mL in 1 BOTTLE · 43386-450-11
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 →