Package 68071-5078-3

Brand: tramadol hydrochloride

Generic: tramadol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-5078-3
Digits Only 6807150783
Product NDC 68071-5078
Product ID 68071-5078_1b466cdb-e4a9-9564-e063-6394a90add37
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-5078-3)

Marketing

Marketing Status
Marketed Since 2019-10-01
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": "1b466cdb-e4a9-9564-e063-6394a90add37", "openfda": {"upc": ["0368071507836"], "unii": ["9N7R477WCK"], "rxcui": ["833713"], "spl_set_id": ["93e129c8-64c4-1f6d-e053-2a95a90ac1f8"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-5078-3)", "package_ndc": "68071-5078-3", "marketing_start_date": "20191001"}], "brand_name": "TRAMADOL HYDROCHLORIDE", "product_id": "68071-5078_1b466cdb-e4a9-9564-e063-6394a90add37", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "68071-5078", "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": "300 mg/1"}], "application_number": "ANDA200503", "marketing_category": "ANDA", "marketing_start_date": "20140818", "listing_expiration_date": "20261231"}