Package 58118-2348-8

Brand: tramadol hydrochloride

Generic: tramadol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 58118-2348-8
Digits Only 5811823488
Product NDC 58118-2348
Product ID 58118-2348_2d7afbeb-0877-e7df-e063-6394a90a2e55
Description

30 TABLET, COATED in 1 BLISTER PACK (58118-2348-8)

Marketing

Marketing Status
Marketed Since 2025-02-06
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": "2d7afbeb-0877-e7df-e063-6394a90a2e55", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["835603"], "spl_set_id": ["728157e2-d153-4ea0-81eb-36599dc7dfda"], "manufacturer_name": ["Clinical Solutions Wholesale, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BLISTER PACK (58118-2348-8)", "package_ndc": "58118-2348-8", "marketing_start_date": "20250206"}], "brand_name": "Tramadol Hydrochloride", "product_id": "58118-2348_2d7afbeb-0877-e7df-e063-6394a90a2e55", "dosage_form": "TABLET, COATED", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "58118-2348", "dea_schedule": "CIV", "generic_name": "Tramadol Hydrochloride", "labeler_name": "Clinical Solutions Wholesale, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tramadol Hydrochloride", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA076003", "marketing_category": "ANDA", "marketing_start_date": "20230213", "listing_expiration_date": "20261231"}