Package 67046-1527-3

Brand: tramadol hydrochloride

Generic: tramadol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67046-1527-3
Digits Only 6704615273
Product NDC 67046-1527
Product ID 67046-1527_2f23c4a9-cdd0-12ee-e063-6294a90af7c0
Description

30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (67046-1527-3)

Marketing

Marketing Status
Marketed Since 2025-02-27
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": "2f23c4a9-cdd0-12ee-e063-6294a90af7c0", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["833709"], "spl_set_id": ["2f23ba6c-89d2-cc42-e063-6394a90aee0a"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (67046-1527-3)", "package_ndc": "67046-1527-3", "marketing_start_date": "20250227"}], "brand_name": "TRAMADOL HYDROCHLORIDE", "product_id": "67046-1527_2f23c4a9-cdd0-12ee-e063-6294a90af7c0", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "67046-1527", "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": "ANDA200503", "marketing_category": "ANDA", "marketing_start_date": "20250227", "listing_expiration_date": "20261231"}