# Nitrofurantoin

NDC: 63629-2464
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

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63629-2464"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63629-2464
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bebbe5d6-f6ec-4191-bad3-b6e933da0688