Package 76420-323-05

Brand: oxycodone and acetaminophen

Generic: oxycodone and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 76420-323-05
Digits Only 7642032305
Product NDC 76420-323
Description

500 TABLET in 1 BOTTLE (76420-323-05)

Marketing

Marketing Status
Marketed Since 2025-04-15
Brand oxycodone and acetaminophen
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": "32cd8c6c-83cf-fa16-e063-6394a90a6f38", "openfda": {"unii": ["C1ENJ2TE6C", "362O9ITL9D"], "rxcui": ["1049214", "1049221", "1049225", "1049635"], "spl_set_id": ["71c7a627-6ed9-4f49-8cdc-b3228c021e64"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (76420-323-01)", "package_ndc": "76420-323-01", "marketing_start_date": "20250415"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (76420-323-05)", "package_ndc": "76420-323-05", "marketing_start_date": "20250415"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (76420-323-30)", "package_ndc": "76420-323-30", "marketing_start_date": "20250415"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (76420-323-60)", "package_ndc": "76420-323-60", "marketing_start_date": "20250415"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (76420-323-90)", "package_ndc": "76420-323-90", "marketing_start_date": "20250415"}], "brand_name": "OXYCODONE AND ACETAMINOPHEN", "product_id": "76420-323_32cd8c6c-83cf-fa16-e063-6394a90a6f38", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "76420-323", "dea_schedule": "CII", "generic_name": "Oxycodone and Acetaminophen", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXYCODONE AND ACETAMINOPHEN", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "OXYCODONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA207419", "marketing_category": "ANDA", "marketing_start_date": "20170411", "listing_expiration_date": "20261231"}