Package 63481-629-70

Brand: percocet

Generic: oxycodone hydrochloride and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 63481-629-70
Digits Only 6348162970
Product NDC 63481-629
Product ID 63481-629_3cbe384a-10a6-4a65-b305-4a466ceed0b4
Description

100 TABLET in 1 BOTTLE (63481-629-70)

Marketing

Marketing Status
Marketed Since 2001-11-30
Brand percocet
Generic oxycodone hydrochloride and acetaminophen
Sample Package No

Linked Drug Pages (1)

PERCOCET ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3cbe384a-10a6-4a65-b305-4a466ceed0b4", "openfda": {"upc": ["0363481623701"], "unii": ["C1ENJ2TE6C", "362O9ITL9D"], "rxcui": ["1049214", "1049221", "1049225", "1049625", "1049635", "1049637", "1049640", "1049642"], "spl_set_id": ["4dd36cf5-8f73-404a-8b1d-3bd53bd90c25"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (63481-629-70)", "package_ndc": "63481-629-70", "marketing_start_date": "20011130"}], "brand_name": "PERCOCET", "product_id": "63481-629_3cbe384a-10a6-4a65-b305-4a466ceed0b4", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "63481-629", "dea_schedule": "CII", "generic_name": "oxycodone hydrochloride and acetaminophen", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PERCOCET", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "OXYCODONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA040330", "marketing_category": "ANDA", "marketing_start_date": "20011130", "listing_expiration_date": "20271231"}