Package 68071-4119-8

Brand: tramadol hydrochloride

Generic: tramadol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-4119-8
Digits Only 6807141198
Product NDC 68071-4119
Description

180 TABLET, COATED in 1 BOTTLE (68071-4119-8)

Marketing

Marketing Status
Marketed Since 2017-10-16
Brand tramadol hydrochloride
Generic tramadol hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2d3fca70-2bc9-7bec-e063-6294a90a8da4", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["835603"], "spl_set_id": ["5babcfcf-331b-5db9-e053-2a91aa0aaf89"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, COATED in 1 BOTTLE (68071-4119-1)", "package_ndc": "68071-4119-1", "marketing_start_date": "20171016"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (68071-4119-3)", "package_ndc": "68071-4119-3", "marketing_start_date": "20171016"}, {"sample": false, "description": "40 TABLET, COATED in 1 BOTTLE (68071-4119-4)", "package_ndc": "68071-4119-4", "marketing_start_date": "20171016"}, {"sample": false, "description": "15 TABLET, COATED in 1 BOTTLE (68071-4119-5)", "package_ndc": "68071-4119-5", "marketing_start_date": "20171016"}, {"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (68071-4119-6)", "package_ndc": "68071-4119-6", "marketing_start_date": "20171016"}, {"sample": false, "description": "84 TABLET, COATED in 1 BOTTLE (68071-4119-7)", "package_ndc": "68071-4119-7", "marketing_start_date": "20171016"}, {"sample": false, "description": "180 TABLET, COATED in 1 BOTTLE (68071-4119-8)", "package_ndc": "68071-4119-8", "marketing_start_date": "20171016"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (68071-4119-9)", "package_ndc": "68071-4119-9", "marketing_start_date": "20171016"}], "brand_name": "Tramadol Hydrochloride", "product_id": "68071-4119_2d3fca70-2bc9-7bec-e063-6294a90a8da4", "dosage_form": "TABLET, COATED", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "68071-4119", "dea_schedule": "CIV", "generic_name": "Tramadol Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "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": "20101115", "listing_expiration_date": "20261231"}