Package 63629-8876-1

Brand: oxycodone and acetaminophen

Generic: oxycodone and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 63629-8876-1
Digits Only 6362988761
Product NDC 63629-8876
Product ID 63629-8876_a09c945c-9621-49a8-9b04-acea348af0cf
Description

100 TABLET in 1 BOTTLE, PLASTIC (63629-8876-1)

Marketing

Marketing Status
Marketed Since 2021-10-01
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": "a09c945c-9621-49a8-9b04-acea348af0cf", "openfda": {"unii": ["362O9ITL9D", "C1ENJ2TE6C"], "rxcui": ["1049214"], "spl_set_id": ["639aba0b-1ef6-415f-9732-ebf52bcc1b86"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (63629-8876-1)", "package_ndc": "63629-8876-1", "marketing_start_date": "20211001"}], "brand_name": "Oxycodone and Acetaminophen", "product_id": "63629-8876_a09c945c-9621-49a8-9b04-acea348af0cf", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "63629-8876", "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"}