Package 70518-4461-0

Brand: tramadol hydrochloride and acetaminophen

Generic: tramadol hydrochloride and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 70518-4461-0
Digits Only 7051844610
Product NDC 70518-4461
Description

60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4461-0)

Marketing

Marketing Status
Marketed Since 2025-08-28
Brand tramadol hydrochloride and acetaminophen
Generic tramadol hydrochloride and acetaminophen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3d6eccec-e115-1d20-e063-6294a90ac7d9", "openfda": {"unii": ["362O9ITL9D", "9N7R477WCK"], "rxcui": ["836395"], "spl_set_id": ["5058c2b0-5c66-4cd2-80a6-7a4678c1fd51"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4461-0)", "package_ndc": "70518-4461-0", "marketing_start_date": "20250828"}], "brand_name": "Tramadol Hydrochloride and Acetaminophen", "product_id": "70518-4461_3d6eccec-e115-1d20-e063-6294a90ac7d9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "70518-4461", "dea_schedule": "CIV", "generic_name": "Tramadol Hydrochloride and Acetaminophen", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tramadol Hydrochloride and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "TRAMADOL HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA207152", "marketing_category": "ANDA", "marketing_start_date": "20250828", "listing_expiration_date": "20261231"}