# Tramadol Hydrochloride

NDC: 58118-2348
Generic name: Tramadol Hydrochloride
Labeler / Manufacturer: Clinical Solutions Wholesale, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20230213

FDA application: ANDA076003

## Active ingredients

- TRAMADOL HYDROCHLORIDE: 50 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"58118-2348"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=58118-2348
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=728157e2-d153-4ea0-81eb-36599dc7dfda