Package 72162-1335-6

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1335-6
Digits Only 7216213356
Product NDC 72162-1335
Product ID 72162-1335_9a8113bd-75c9-47bf-bbda-0388fe60e05f
Description

60 TABLET in 1 BOTTLE (72162-1335-6)

Marketing

Marketing Status
Marketed Since 2023-03-30
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": "9a8113bd-75c9-47bf-bbda-0388fe60e05f", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049683"], "spl_set_id": ["a1e539ba-2cb5-4815-8c58-37abfd978fa5"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET in 1 BOTTLE (72162-1335-2)", "package_ndc": "72162-1335-2", "marketing_start_date": "20230330"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (72162-1335-3)", "package_ndc": "72162-1335-3", "marketing_start_date": "20230330"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (72162-1335-6)", "package_ndc": "72162-1335-6", "marketing_start_date": "20230330"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72162-1335-9)", "package_ndc": "72162-1335-9", "marketing_start_date": "20230330"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "72162-1335_9a8113bd-75c9-47bf-bbda-0388fe60e05f", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72162-1335", "dea_schedule": "CII", "generic_name": "Oxycodone Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA091490", "marketing_category": "ANDA", "marketing_start_date": "20140908", "listing_expiration_date": "20261231"}