Package 0121-0826-01

Brand: OXYCODONE HYDROCHLORIDE

Generic: OXYCODONE HYDROCHLORIDE
NDC Package

Package Facts

Identity

Package NDC 0121-0826-01
Digits Only 0121082601
Product NDC 0121-0826
Product ID 0121-0826_1109a611-cf88-4447-b2ac-de7fc081a094
Description

1 BOTTLE in 1 CARTON (0121-0826-01) / 30 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2018-06-04
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": "1109a611-cf88-4447-b2ac-de7fc081a094", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049615"], "spl_set_id": ["54ece3f4-6ba1-411e-a0c6-2141a400b71a"], "manufacturer_name": ["PAI Holdings, LLC dba PAI Pharma"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0121-0826-01)  / 30 mL in 1 BOTTLE", "package_ndc": "0121-0826-01", "marketing_start_date": "20180604"}], "brand_name": "OXYCODONE HYDROCHLORIDE", "product_id": "0121-0826_1109a611-cf88-4447-b2ac-de7fc081a094", "dosage_form": "SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0121-0826", "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": "100 mg/5mL"}], "application_number": "ANDA206822", "marketing_category": "ANDA", "marketing_start_date": "20180604", "listing_expiration_date": "20261231"}