# Tapentadol Hydrochloride

NDC: 72205-369
Generic name: Tapentadol Hydrochloride
Labeler / Manufacturer: Novadoz Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20260903

FDA application: ANDA220865

## Active ingredients

- TAPENTADOL HYDROCHLORIDE: 50 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72205-369"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72205-369
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d4c5938a-68f0-46d2-9bad-8988d5724b09