Package 58118-0377-8

Brand: tramadol hydrochloride

Generic: tramadol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 58118-0377-8
Digits Only 5811803778
Product NDC 58118-0377
Product ID 58118-0377_0e85bc3d-4f3c-00d3-e063-6294a90a847a
Description

30 TABLET in 1 BLISTER PACK (58118-0377-8)

Marketing

Marketing Status
Marketed Since 2020-05-26
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": "0e85bc3d-4f3c-00d3-e063-6294a90a847a", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["835603"], "spl_set_id": ["88e66c0e-22a0-4ca7-bbff-c2f63df57c96"], "manufacturer_name": ["Clinical Solutions Wholesale, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (58118-0377-8)", "package_ndc": "58118-0377-8", "marketing_start_date": "20200526"}], "brand_name": "tramadol hydrochloride", "product_id": "58118-0377_0e85bc3d-4f3c-00d3-e063-6294a90a847a", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "58118-0377", "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": "ANDA075964", "marketing_category": "ANDA", "marketing_start_date": "20020622", "listing_expiration_date": "20261231"}