# Nitrofurantoin

NDC: 70069-829
Generic name: Nitrofurantoin
Labeler / Manufacturer: Somerset Therapeutics, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: FOR SUSPENSION
Routes: ORAL
Marketing started: 20250226

FDA application: ANDA208909

## Active ingredients

- NITROFURANTOIN: 25 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70069-829"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70069-829
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=dd99ba40-edff-47c3-9ee4-7e5b7774e5b5