# Tramadol Hydrochloride and Acetaminophen

NDC: 65862-922
Generic name: Tramadol Hydrochloride and Acetaminophen
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20170322

FDA application: ANDA207152

## Active ingredients

- ACETAMINOPHEN: 325 mg/1
- TRAMADOL HYDROCHLORIDE: 37.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65862-922"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65862-922
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6c2894df-eeeb-4b22-ab32-8ce1601bfdfa