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
- 68071-2928_58f2e453-4c4f-7278-e063-6394a90a0006
- Product NDC
- 68071-2928
- Form
- CAPSULE
- Composition / generic term
- Nitrofurantoin
- Labeler
- NuCare Pharmaceuticals,Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180101
- 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
- 20 CAPSULE in 1 BOTTLE (68071-2928-2) · 68071-2928-2
- 14 CAPSULE in 1 BOTTLE (68071-2928-4) · 68071-2928-4
- 6 CAPSULE in 1 BOTTLE (68071-2928-6) · 68071-2928-6
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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