United States · FDA National Drug Code directory
Nitrofurantion
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
- 57664-232_4ed13848-1151-c63a-e063-6394a90a3a05
- Product NDC
- 57664-232
- Form
- CAPSULE
- Composition / generic term
- Nitrofurantion
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160415
- Source listing expiry
- 20271231
Source-listed ingredients
- NITROFURANTOIN — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 CAPSULE in 1 BOTTLE (57664-232-18) · 57664-232-18
- 100 CAPSULE in 1 BOTTLE (57664-232-88) · 57664-232-88
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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