Package 67046-1541-3

Brand: tramadol hydrochloride

Generic: tramadol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67046-1541-3
Digits Only 6704615413
Product NDC 67046-1541
Product ID 67046-1541_3135a0e3-6e29-4091-e063-6394a90a52cb
Description

30 TABLET, COATED in 1 BLISTER PACK (67046-1541-3)

Marketing

Marketing Status
Marketed Since 2025-03-25
Brand tramadol hydrochloride
Generic tramadol hydrochloride
Sample Package No

Linked Drug Pages (1)

Tramadol Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3135a0e3-6e29-4091-e063-6394a90a52cb", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["2179635"], "spl_set_id": ["3135a131-5f2d-3775-e063-6394a90a4322"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BLISTER PACK (67046-1541-3)", "package_ndc": "67046-1541-3", "marketing_start_date": "20250325"}], "brand_name": "Tramadol Hydrochloride", "product_id": "67046-1541_3135a0e3-6e29-4091-e063-6394a90a52cb", "dosage_form": "TABLET, COATED", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "67046-1541", "dea_schedule": "CIV", "generic_name": "Tramadol Hydrochloride", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tramadol Hydrochloride", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA208708", "marketing_category": "ANDA", "marketing_start_date": "20250325", "listing_expiration_date": "20261231"}