United States · FDA National Drug Code directory

Nitrofurantoin (monohydrate/macrocrystals)

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
68071-3593_45a09574-d7e4-1932-e063-6394a90a8765
Product NDC
68071-3593
Form
CAPSULE
Composition / generic term
Nitrofurantoin (monohydrate/macrocrystals)
Labeler
NuCare Pharmaceuticals,Inc.
Marketing category
ANDA
Marketing start / end (source format)
20230914
Source listing expiry
20261231

Source-listed ingredients

  • NITROFURANTOIN MONOHYDRATE — 75 mg/1
  • NITROFURANTOIN — 25 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 2 CAPSULE in 1 BOTTLE (68071-3593-2) · 68071-3593-2
  • 6 CAPSULE in 1 BOTTLE (68071-3593-6) · 68071-3593-6

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 →