Package 0121-0827-04

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0121-0827-04
Digits Only 0121082704
Product NDC 0121-0827
Description

118 mL in 1 BOTTLE (0121-0827-04)

Marketing

Marketing Status
Marketed Since 2019-04-08
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": "1685138a-dd0b-4e6e-b14d-a1132eef8b34", "openfda": {"unii": ["C1ENJ2TE6C"], "spl_set_id": ["73b063b5-24b7-40bf-bc2a-c0e1bfaf61d1"], "manufacturer_name": ["PAI Holdings, LLC dba PAI Pharma"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "118 mL in 1 BOTTLE (0121-0827-04)", "package_ndc": "0121-0827-04", "marketing_start_date": "20190408"}, {"sample": false, "description": "500 mL in 1 BOTTLE (0121-0827-16)", "package_ndc": "0121-0827-16", "marketing_start_date": "20190408"}], "brand_name": "OXYCODONE HYDROCHLORIDE", "product_id": "0121-0827_1685138a-dd0b-4e6e-b14d-a1132eef8b34", "dosage_form": "SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0121-0827", "dea_schedule": "CII", "generic_name": "OXYCODONE HYDROCHLORIDE", "labeler_name": "PAI Holdings, LLC dba PAI Pharma", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXYCODONE HYDROCHLORIDE", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/5mL"}], "application_number": "ANDA206914", "marketing_category": "ANDA", "marketing_start_date": "20190408", "listing_expiration_date": "20271231"}