# Nitrofurantoin

NDC: 71335-2320
Generic name: Nitrofurantoin
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20180101

FDA application: ANDA208516

## 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:"71335-2320"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-2320
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=75dab97e-59b4-447c-a8c9-b4d5a970098f