# Tramadol Hydrochloride

NDC: 80425-0276
Generic name: Tramadol Hydrochloride
Labeler / Manufacturer: Advanced Rx Pharmacy of Tennessee, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20230217

FDA application: ANDA208708

## 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:"80425-0276"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80425-0276
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f4ea18b0-2cbd-0d42-e053-2995a90a9264