Package 67296-0425-1

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67296-0425-1
Digits Only 6729604251
Product NDC 67296-0425
Product ID 67296-0425_3252751e-38fb-6056-e063-6394a90a1340
Description

20 TABLET in 1 BOTTLE (67296-0425-1)

Marketing

Marketing Status
Marketed Since 2019-01-01
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": "3252751e-38fb-6056-e063-6394a90a1340", "openfda": {"upc": ["0367296042542"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1049621"], "spl_set_id": ["92614a3a-331d-16ad-e053-2a95a90a47cc"], "manufacturer_name": ["RedPharm Drug, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (67296-0425-1)", "package_ndc": "67296-0425-1", "marketing_start_date": "20190101"}, {"sample": false, "description": "4 TABLET in 1 BOTTLE (67296-0425-4)", "package_ndc": "67296-0425-4", "marketing_start_date": "20190101"}], "brand_name": "OXYCODONE HYDROCHLORIDE", "product_id": "67296-0425_3252751e-38fb-6056-e063-6394a90a1340", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "67296-0425", "dea_schedule": "CII", "generic_name": "oxycodone hydrochloride", "labeler_name": "RedPharm Drug, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXYCODONE HYDROCHLORIDE", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA076758", "marketing_category": "ANDA", "marketing_start_date": "20090730", "listing_expiration_date": "20261231"}