# Tramadol Hydrochloride

NDC: 33342-271
Generic name: Tramadol Hydrochloride
Labeler / Manufacturer: Macleods Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20250131

FDA application: ANDA209404

## Active ingredients

- TRAMADOL HYDROCHLORIDE: 300 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"33342-271"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=33342-271
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a07ed444-54e4-4d45-b6a1-6ea2f6dedc61