Package 72162-1336-1

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1336-1
Digits Only 7216213361
Product NDC 72162-1336
Product ID 72162-1336_fa7d97f3-3d54-418b-861e-0facba5e2787
Description

100 TABLET in 1 BOTTLE, PLASTIC (72162-1336-1)

Marketing

Marketing Status
Marketed Since 2024-07-16
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": "fa7d97f3-3d54-418b-861e-0facba5e2787", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049611"], "spl_set_id": ["0e4dd113-87ab-4a5d-846a-446db3cfd469"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72162-1336-1)", "package_ndc": "72162-1336-1", "marketing_start_date": "20240716"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "72162-1336_fa7d97f3-3d54-418b-861e-0facba5e2787", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72162-1336", "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": "15 mg/1"}], "application_number": "ANDA091490", "marketing_category": "ANDA", "marketing_start_date": "20140908", "listing_expiration_date": "20261231"}