Package 72189-095-90

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72189-095-90
Digits Only 7218909590
Product NDC 72189-095
Product ID 72189-095_36d68732-0635-1380-e063-6394a90a69c6
Description

90 TABLET in 1 BOTTLE (72189-095-90)

Marketing

Marketing Status
Marketed Since 2020-06-15
Brand oxycodone hydrochloride
Generic oxycodone hydrochloride
Sample Package No

Linked Drug Pages (1)

OXYCODONE HYDROCHLORIDE, OXYCODONE AND ACETAMINOPHEN ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "36d68732-0635-1380-e063-6394a90a69c6", "openfda": {"unii": ["C1ENJ2TE6C", "362O9ITL9D"], "rxcui": ["1049214", "1049225", "1049621", "1049683"], "spl_set_id": ["a8206207-ad09-83df-e053-2995a90a78b7"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-095-30)", "package_ndc": "72189-095-30", "marketing_start_date": "20200615"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (72189-095-60)", "package_ndc": "72189-095-60", "marketing_start_date": "20200615"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-095-90)", "package_ndc": "72189-095-90", "marketing_start_date": "20200615"}], "brand_name": "OXYCODONE HYDROCHLORIDE", "product_id": "72189-095_36d68732-0635-1380-e063-6394a90a69c6", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72189-095", "dea_schedule": "CII", "generic_name": "OXYCODONE HYDROCHLORIDE", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXYCODONE HYDROCHLORIDE", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA204021", "marketing_category": "ANDA", "marketing_start_date": "20200615", "listing_expiration_date": "20261231"}