Package 63629-2190-1
Brand: endocet
Generic: oxycodone and acetaminophenPackage Facts
Identity
Package NDC
63629-2190-1
Digits Only
6362921901
Product NDC
63629-2190
Description
100 TABLET in 1 BOTTLE, PLASTIC (63629-2190-1)
Marketing
Marketing Status
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": "3b8ef94a-da42-46b5-9fa9-2fac9ed6e7c3", "openfda": {"unii": ["362O9ITL9D", "C1ENJ2TE6C"], "rxcui": ["1049225", "1049227"], "spl_set_id": ["3b8ef94a-da42-46b5-9fa9-2fac9ed6e7c3"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (63629-2190-1)", "package_ndc": "63629-2190-1", "marketing_start_date": "20240808"}], "brand_name": "ENDOCET", "product_id": "63629-2190_3b8ef94a-da42-46b5-9fa9-2fac9ed6e7c3", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "63629-2190", "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": "7.5 mg/1"}], "application_number": "ANDA040330", "marketing_category": "ANDA", "marketing_start_date": "20030306", "listing_expiration_date": "20261231"}