# NITROFURANTOIN

NDC: 46708-389
Generic name: NITROFURANTOIN
Labeler / Manufacturer: Alembic Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20210701

FDA application: ANDA211935

## Active ingredients

- NITROFURANTOIN: 25 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"46708-389"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=46708-389
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=152e4fe2-7665-4725-af76-b241bd816937