Package 68071-5169-2

Brand: oxycodone and acetaminophen

Generic: oxycodone and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 68071-5169-2
Digits Only 6807151692
Product NDC 68071-5169
Product ID 68071-5169_1b567965-f9d1-becb-e063-6394a90a030e
Description

20 TABLET in 1 BOTTLE (68071-5169-2)

Marketing

Marketing Status
Marketed Since 2020-02-10
Brand oxycodone and acetaminophen
Generic oxycodone and acetaminophen
Sample Package No

Linked Drug Pages (1)

Oxycodone and Acetaminophen ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1b567965-f9d1-becb-e063-6394a90a030e", "openfda": {"upc": ["0368071516920"], "unii": ["362O9ITL9D", "C1ENJ2TE6C"], "rxcui": ["1049221"], "spl_set_id": ["9e4024f4-0f60-dfef-e053-2995a90ac366"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (68071-5169-2)", "package_ndc": "68071-5169-2", "marketing_start_date": "20200210"}], "brand_name": "Oxycodone and Acetaminophen", "product_id": "68071-5169_1b567965-f9d1-becb-e063-6394a90a030e", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "68071-5169", "dea_schedule": "CII", "generic_name": "Oxycodone and Acetaminophen", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA207419", "marketing_category": "ANDA", "marketing_start_date": "20170411", "listing_expiration_date": "20261231"}