Package 68071-3600-4

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-3600-4
Digits Only 6807136004
Product NDC 68071-3600
Product ID 68071-3600_17f796b6-3f89-c988-e063-6394a90a7cb8
Description

4 TABLET in 1 BOTTLE (68071-3600-4)

Marketing

Marketing Status
Marketed Since 2024-05-08
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": "17f796b6-3f89-c988-e063-6394a90a7cb8", "openfda": {"upc": ["0368071360042"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1049621"], "spl_set_id": ["17f7946d-e889-b736-e063-6394a90a42e0"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET in 1 BOTTLE (68071-3600-4)", "package_ndc": "68071-3600-4", "marketing_start_date": "20240508"}], "brand_name": "OXYCODONE HYDROCHLORIDE", "product_id": "68071-3600_17f796b6-3f89-c988-e063-6394a90a7cb8", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "68071-3600", "dea_schedule": "CII", "generic_name": "OXYCODONE HYDROCHLORIDE", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXYCODONE HYDROCHLORIDE", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA091393", "marketing_category": "ANDA", "marketing_start_date": "20131018", "listing_expiration_date": "20261231"}