# Tramadol Hydrochloride

NDC: 80425-0548
Generic name: Tramadol Hydrochloride
Labeler / Manufacturer: Advanced Rx of Tennessee, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20250827

FDA application: ANDA211825

## Active ingredients

- TRAMADOL HYDROCHLORIDE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"80425-0548"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80425-0548
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3d719560-7449-f970-e063-6294a90a9bd8