# Nitrofurantoin (monohydrate/macrocrystals)

NDC: 70518-4358
Generic name: Nitrofurantoin (monohydrate/macrocrystals)
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20250616

FDA application: ANDA217357

## Active ingredients

- NITROFURANTOIN: 25 mg/1
- NITROFURANTOIN MONOHYDRATE: 75 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-4358"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-4358
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4553ccc1-0bad-4c75-aae2-1a1c87bc8db0