Package 63629-8879-2

Brand: oxycodone and acetaminophen

Generic: oxycodone and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 63629-8879-2
Digits Only 6362988792
Product NDC 63629-8879
Description

90 TABLET in 1 BOTTLE, PLASTIC (63629-8879-2)

Marketing

Marketing Status
Marketed Since 2021-10-04
Brand oxycodone and acetaminophen
Generic oxycodone and acetaminophen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f15258bd-bf40-4307-8af1-ad8f84440f6d", "openfda": {"unii": ["362O9ITL9D", "C1ENJ2TE6C"], "rxcui": ["1049214"], "spl_set_id": ["626b7834-edb8-4d13-af5c-fff97d4eb9de"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (63629-8879-1)", "package_ndc": "63629-8879-1", "marketing_start_date": "20211004"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (63629-8879-2)", "package_ndc": "63629-8879-2", "marketing_start_date": "20211004"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (63629-8879-3)", "package_ndc": "63629-8879-3", "marketing_start_date": "20211004"}], "brand_name": "Oxycodone and Acetaminophen", "product_id": "63629-8879_f15258bd-bf40-4307-8af1-ad8f84440f6d", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "63629-8879", "dea_schedule": "CII", "generic_name": "Oxycodone and Acetaminophen", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "OXYCODONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA201278", "marketing_category": "ANDA", "marketing_start_date": "20140828", "listing_expiration_date": "20261231"}