# Pentoxifylline

NDC: 16571-856
Generic name: Pentoxifylline
Labeler / Manufacturer: Rising Pharma Holdings, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20240611

FDA application: ANDA074425

## Active ingredients

- PENTOXIFYLLINE: 400 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"16571-856"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16571-856
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cd840a2c-2a0e-4b2b-84ff-a0406bb6fa37