# Tramadol Hydrochloride

NDC: 60760-772
Generic name: Tramadol Hydrochloride
Labeler / Manufacturer: ST. MARY'S MEDICAL PARK PHARMACY
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20221228

FDA application: ANDA203494

## 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:"60760-772"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60760-772
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f2f421ab-35ae-7637-e053-2995a90a40e0