# Methenamine Hippurate

NDC: 70954-959
Generic name: Methenamine Hippurate
Labeler / Manufacturer: ANI Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20260727

FDA application: NDA017681

## Active ingredients

- METHENAMINE HIPPURATE: 1 g/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70954-959"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70954-959
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a3eeacd4-1983-49ec-a60d-3abaf505ce57