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
72603-196_1080bf1e-86d4-4f7a-9b1b-2823a389dbcc
Product NDC
72603-196
Form
CAPSULE
Composition / generic term
Nitrofurantoin (monohydrate/macrocrystals)
Labeler
NorthStar RxLLC
Marketing category
ANDA
Marketing start / end (source format)
20231201
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

  • 100 CAPSULE in 1 BOTTLE (72603-196-01) · 72603-196-01

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.

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Nitrofurantoin (monohydrate/macrocrystals) — United States | Molindra Medicines