# Tramadol Hydrochloride

NDC: 68071-4119
Generic name: Tramadol Hydrochloride
Labeler / Manufacturer: NuCare Pharmaceuticals,Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20101115

FDA application: ANDA076003

## Active ingredients

- TRAMADOL HYDROCHLORIDE: 50 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68071-4119"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-4119
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5babcfcf-331b-5db9-e053-2a91aa0aaf89