# NITROFURANTOIN

NDC: 70377-118
Generic name: NITROFURANTOIN
Labeler / Manufacturer: Biocon Pharma Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUSPENSION
Routes: ORAL
Marketing started: 20241115

FDA application: ANDA218346

## Active ingredients

- NITROFURANTOIN: 25 mg/5mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70377-118"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70377-118
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=68c718a7-2e8f-288c-37d2-053372ee61b9