# Nitrofurantoin (monohydrate/macrocrystals)

NDC: 72789-242
Generic name: Nitrofurantoin (monohydrate/macrocrystals)
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20050406

FDA application: ANDA077066

## 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:"72789-242"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72789-242
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=643cdcff-8599-4326-b3ca-d9fd270e0fc2