# Tramadol Hydrochloride and Acetaminophen

NDC: 50268-774
Generic name: Tramadol Hydrochloride and Acetaminophen
Labeler / Manufacturer: AvPAK
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20150114
Marketing ended: 20270331
FDA application: ANDA090485

## Active ingredients

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

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50268-774"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50268-774
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=244f6e5d-e1b4-ba8b-ca6f-af2d8a31d5f0