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
- 70518-3717_596c5a11-5d18-f6eb-e063-6394a90a58eb
- Product NDC
- 70518-3717
- Form
- CAPSULE
- Composition / generic term
- Nitrofurantoin
- Labeler
- REMEDYREPACK INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230418
- Source listing expiry
- 20271231
Source-listed ingredients
- NITROFURANTOIN — 25 mg/1
- NITROFURANTOIN MONOHYDRATE — 75 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 14 CAPSULE in 1 BOTTLE, PLASTIC (70518-3717-0) · 70518-3717-0
- 10 CAPSULE in 1 BOTTLE, PLASTIC (70518-3717-2) · 70518-3717-2
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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