Package 63629-2187-1

Brand: endocet

Generic: oxycodone and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 63629-2187-1
Digits Only 6362921871
Product NDC 63629-2187
Description

100 TABLET in 1 BOTTLE, PLASTIC (63629-2187-1)

Marketing

Marketing Status
Marketed Since 2024-08-08
Brand endocet
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": "9996553a-f4d5-4c32-adc6-0543d818a5fd", "openfda": {"unii": ["362O9ITL9D", "C1ENJ2TE6C"], "rxcui": ["1049214", "1049216"], "spl_set_id": ["1b847d11-3382-458c-ae65-579d0b0d9a4b"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (63629-2187-1)", "package_ndc": "63629-2187-1", "marketing_start_date": "20240808"}], "brand_name": "ENDOCET", "product_id": "63629-2187_9996553a-f4d5-4c32-adc6-0543d818a5fd", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "63629-2187", "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": "10 mg/1"}], "application_number": "ANDA040330", "marketing_category": "ANDA", "marketing_start_date": "20030306", "listing_expiration_date": "20261231"}