# Tramadol Hydrochloride

NDC: 68180-383
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: 20110926

FDA application: ANDA200503

## Active ingredients

- TRAMADOL HYDROCHLORIDE: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68180-383"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68180-383
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3e0ccb95-3e8e-477c-b4d2-6060ee05f930