Package 68084-354-01

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68084-354-01
Digits Only 6808435401
Product NDC 68084-354
Product ID 68084-354_4160b55c-48e1-5cb4-e063-6294a90a1d7d
Description

100 BLISTER PACK in 1 CARTON (68084-354-01) / 1 TABLET in 1 BLISTER PACK (68084-354-11)

Marketing

Marketing Status
Marketed Since 2009-12-04
Brand oxycodone hydrochloride
Generic oxycodone hydrochloride
Sample Package No

Linked Drug Pages (1)

OXYCODONE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4160b55c-48e1-5cb4-e063-6294a90a1d7d", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049611", "1049618", "1049621", "1049683"], "spl_set_id": ["aa7ac2bf-d9ed-445d-b394-4d3fe39780ca"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (68084-354-01)  / 1 TABLET in 1 BLISTER PACK (68084-354-11)", "package_ndc": "68084-354-01", "marketing_start_date": "20091204"}], "brand_name": "OXYCODONE HYDROCHLORIDE", "product_id": "68084-354_4160b55c-48e1-5cb4-e063-6294a90a1d7d", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "68084-354", "dea_schedule": "CII", "generic_name": "OXYCODONE HYDROCHLORIDE", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXYCODONE HYDROCHLORIDE", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA091393", "marketing_category": "ANDA", "marketing_start_date": "20091204", "listing_expiration_date": "20261231"}