Package 63629-1912-1

Brand: oxycodone and acetaminophen

Generic: oxycodone and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 63629-1912-1
Digits Only 6362919121
Product NDC 63629-1912
Product ID 63629-1912_5b8657fe-0961-420e-ab95-11906c0bff70
Description

500 TABLET in 1 BOTTLE (63629-1912-1)

Marketing

Marketing Status
Marketed Since 2019-03-15
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": "5b8657fe-0961-420e-ab95-11906c0bff70", "openfda": {"unii": ["362O9ITL9D", "C1ENJ2TE6C"], "rxcui": ["1049225"], "spl_set_id": ["5513980d-69e8-4f12-b881-56f2d80db951"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (63629-1912-1)", "package_ndc": "63629-1912-1", "marketing_start_date": "20190315"}], "brand_name": "Oxycodone and Acetaminophen", "product_id": "63629-1912_5b8657fe-0961-420e-ab95-11906c0bff70", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "63629-1912", "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": "7.5 mg/1"}], "application_number": "ANDA207419", "marketing_category": "ANDA", "marketing_start_date": "20170411", "listing_expiration_date": "20261231"}