# VENXXIVA

NDC: 70709-121
Generic name: tiopronin
Labeler / Manufacturer: Cycle Pharmaceuticals Ltd.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20250122

FDA application: ANDA216990

## Active ingredients

- TIOPRONIN: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70709-121"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70709-121
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=02e24443-04c6-4b98-a395-49aec4a468de