# TRAMADOL HYDROCHLORIDE

NDC: 76420-246
Generic name: TRAMADOL HYDROCHLORIDE
Labeler / Manufacturer: Asclemed USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20111212

FDA application: ANDA201384

## Active ingredients

- TRAMADOL HYDROCHLORIDE: 300 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"76420-246"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76420-246
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=dce0d21e-e4c2-4875-a2ce-9d53df190b80