# TRAMADOL HYDROCHLORIDE

NDC: 68180-698
Generic name: TRAMADOL HYDROCHLORIDE
Labeler / Manufacturer: Lupin Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20140819

FDA application: ANDA200503

## Active ingredients

- TRAMADOL HYDROCHLORIDE: 200 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68180-698"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68180-698
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=46bb9ae6-3ee8-463c-badb-c7a45a89b84b