# Nitrofurantoin Mono

NDC: 54348-849
Generic name: NITROFURANTOIN MONOHYDRATE
Labeler / Manufacturer: PharmPak, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20190710

FDA application: NDA020064

## 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:"54348-849"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=54348-849
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d9840719-271f-42a9-a5c9-3e039ec8fbac