# Tramadol Hydrochloride

NDC: 52817-196
Generic name: Tramadol Hydrochloride
Labeler / Manufacturer: TRUPHARMA LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20200224

FDA application: ANDA208708

## Active ingredients

- TRAMADOL HYDROCHLORIDE: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"52817-196"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=52817-196
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=61fb5ba7-6896-4ee4-83de-caee69b06a8e