# Tapentadol Hydrochloride

NDC: 70954-801
Generic name: Tapentadol Hydrochloride
Labeler / Manufacturer: ANI Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20260713

FDA application: ANDA219119

## Active ingredients

- TAPENTADOL HYDROCHLORIDE: 20 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70954-801"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70954-801
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e0ecb809-6a55-4afe-b981-b8f174e5c344