# Nitrofurantoin Monohydrate/ Macrocrystalline

NDC: 70518-0265
Generic name: Nitrofurantoin Monohydrate/Macrocrystalline
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20170228

FDA application: NDA020064

## Active ingredients

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

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-0265"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-0265
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a4afd48b-003f-4ffa-9ca0-9432b8b0e22b