# Flavoxate Hydrochloride

NDC: 24658-720
Generic name: Flavoxate Hydrochloride
Labeler / Manufacturer: PuraCap Laboratories LLC dba Blu Pharmaceuticals
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20161215

FDA application: ANDA076835

## Active ingredients

- FLAVOXATE HYDROCHLORIDE: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"24658-720"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=24658-720
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f6a06eda-2480-4c0d-8d1e-9e3e89d3ee88