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
76420-195_e9294cf2-886b-1f04-e053-2995a90a3984
Product NDC
76420-195
Form
CAPSULE
Composition / generic term
Nitrofurantoin (monohydrate/macrocrystals)
Labeler
Asclemed USA, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20050406
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 (76420-195-01) · 76420-195-01
  • 10 CAPSULE in 1 BOTTLE (76420-195-10) · 76420-195-10
  • 14 CAPSULE in 1 BOTTLE (76420-195-14) · 76420-195-14
  • 20 CAPSULE in 1 BOTTLE (76420-195-20) · 76420-195-20
  • 30 CAPSULE in 1 BOTTLE (76420-195-30) · 76420-195-30
  • 60 CAPSULE in 1 BOTTLE (76420-195-60) · 76420-195-60
  • 90 CAPSULE in 1 BOTTLE (76420-195-90) · 76420-195-90

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 →