# Nitrofurantion

NDC: 57664-233
Generic name: Nitrofurantion
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20160415

FDA application: ANDA201722

## Active ingredients

- NITROFURANTOIN: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"57664-233"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=57664-233
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=05f25774-f56a-48ef-bac3-8af663f8581a