# NITROFURANTOIN

NDC: 65862-929
Generic name: Nitrofurantoin (Monohydrate/Macrocrystals)
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20230330

FDA application: ANDA209225

## Active ingredients

- NITROFURANTOIN: 25 mg/1
- NITROFURANTOIN MONOHYDRATE: 75 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65862-929"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65862-929
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=788f1fe3-d8a1-42cc-9280-07f842da34ea