# NITROFURANTOIN

NDC: 72189-179
Generic name: NITROFURANTOIN
Labeler / Manufacturer: Directrx
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20220118

FDA application: ANDA077066

## 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:"72189-179"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72189-179
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d4385368-46d6-8397-e053-2a95a90a8d68