Package 63629-2189-1

Brand: endocet

Generic: oxycodone and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 63629-2189-1
Digits Only 6362921891
Product NDC 63629-2189
Product ID 63629-2189_9bc5874c-7b6b-43a1-9433-a0746dd1e27e
Description

500 TABLET in 1 BOTTLE (63629-2189-1)

Marketing

Marketing Status
Marketed Since 2000-05-26
Brand endocet
Generic oxycodone and acetaminophen
Sample Package No

Linked Drug Pages (1)

ENDOCET ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9bc5874c-7b6b-43a1-9433-a0746dd1e27e", "openfda": {"unii": ["362O9ITL9D", "C1ENJ2TE6C"], "rxcui": ["1049221", "1049223"], "spl_set_id": ["029deff5-98f3-4f4c-9f03-d7436dabdf17"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (63629-2189-1)", "package_ndc": "63629-2189-1", "marketing_start_date": "20000526"}], "brand_name": "ENDOCET", "product_id": "63629-2189_9bc5874c-7b6b-43a1-9433-a0746dd1e27e", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "63629-2189", "dea_schedule": "CII", "generic_name": "Oxycodone and Acetaminophen", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ENDOCET", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA040330", "marketing_category": "ANDA", "marketing_start_date": "20000526", "listing_expiration_date": "20261231"}