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
- 68788-8258_86ac0486-a85c-419b-8a46-ec0ef2f82d8f
- Product NDC
- 68788-8258
- Form
- CAPSULE
- Composition / generic term
- Nitrofurantoin
- Labeler
- Preferred Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220916
- 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
- 10 CAPSULE in 1 BOTTLE (68788-8258-0) · 68788-8258-0
- 14 CAPSULE in 1 BOTTLE (68788-8258-1) · 68788-8258-1
- 28 CAPSULE in 1 BOTTLE (68788-8258-8) · 68788-8258-8
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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