Package 76420-764-30

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 76420-764-30
Digits Only 7642076430
Product NDC 76420-764
Description

30 TABLET in 1 BOTTLE (76420-764-30)

Marketing

Marketing Status
Marketed Since 2024-06-25
Brand oxycodone hydrochloride
Generic oxycodone hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1bb160c8-a76d-7033-e063-6294a90adbef", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049611", "1049618", "1049621"], "spl_set_id": ["1bb147d4-1ab6-dd70-e063-6394a90a67a8"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (76420-764-01)", "package_ndc": "76420-764-01", "marketing_start_date": "20240625"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (76420-764-05)", "package_ndc": "76420-764-05", "marketing_start_date": "20240625"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (76420-764-10)", "package_ndc": "76420-764-10", "marketing_start_date": "20240625"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (76420-764-20)", "package_ndc": "76420-764-20", "marketing_start_date": "20240625"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (76420-764-30)", "package_ndc": "76420-764-30", "marketing_start_date": "20240625"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (76420-764-60)", "package_ndc": "76420-764-60", "marketing_start_date": "20240625"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (76420-764-90)", "package_ndc": "76420-764-90", "marketing_start_date": "20240625"}], "brand_name": "Oxycodone hydrochloride", "product_id": "76420-764_1bb160c8-a76d-7033-e063-6294a90adbef", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "76420-764", "dea_schedule": "CII", "generic_name": "Oxycodone hydrochloride", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA202116", "marketing_category": "ANDA", "marketing_start_date": "20111230", "listing_expiration_date": "20261231"}